Celin

Quick links to important sections

Medically reviewed

Laura Arias

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Celin

Quick Facts: Celin (Sodium Ascorbate)

Property Description
Active Ingredient Sodium Ascorbate
Form Oral Preparation (Tablet, Chewable Tablet)
Pharmacological Class Nutritional Supplement / Vitamin Preparation
Common Use Ascorbic Acid Supplementation
Origin Synthetic Derivative

Celin: Identity, Classification, and Composition

Celin is a widely utilized nutritional supplement classified within the high-level group of vitamin preparations, providing a source of Vitamin C. Its core identity is defined by the active ingredient, Sodium Ascorbate (CAS: 134-03-2), which is the sodium salt form of the essential nutrient L-Ascorbic Acid. As a single-ingredient product, Celin is primarily delivered as an oral preparation, commonly formulated into a tablet or chewable tablet, often positioned for both pediatric patients and adults due to its form and profile. This classification confirms the preparation’s role as a fundamental support agent, providing a reliable source of an essential component.


Formulation and General Purpose of the Essential Nutrient

The distinguishing feature of the Celin preparation is the use of Sodium Ascorbate, a synthetic derivative chemically classified as a mineral ascorbate. This compound is produced to create a buffered formulation with a near-neutral pH, a key characteristic that sets it apart from the highly acidic pure Ascorbic Acid and is often preferred for enhanced gastrointestinal tolerability. This buffered quality is clinically recognized for potentially improving compliance in individuals with sensitive stomachs. The general purpose of this preparation is to provide necessary metabolic support, as this essential nutrient functions primarily as a powerful reducing agent and cofactor. By maintaining adequate Ascorbic Acid levels, Celin is commonly used as a daily regimen to support structural integrity and promote cellular defense.

Regulatory References

  1. Sodium Ascorbate
  2. L-Ascorbic Acid
  3. Ascorbic Acid Supplementation
  4. essential nutrient
  5. MedlinePlus Information

What side effects are possible with Celin?

Possible Side Effects and Safety Information

The official safety profile for Celin (Sodium Ascorbate) outlines adverse reactions primarily classified by the systems they affect, with general effects being Common at higher doses, while severe reactions are Very Rare in the general population.


Adverse Reaction Scope

Category Regulatory Documentation Note
System-Organ Classes Effects predominantly involve Gastrointestinal Disorders (e.g., diarrhea, heartburn, stomach cramps) and Renal and Urinary Disorders.
Common Reactions Headache, nausea, vomiting, fatigue, and flushing are generally reported as common, especially with increased intake.
Dose-Related Patterns The risk of serious reactions, such as Nephrolithiasis (kidney stones) and Oxalate Nephropathy, is strongly associated with prolonged use of high doses (e.g., intakes over 2,000 mg daily).

Serious Adverse Reactions and Specific Safety Considerations

Official labeling documents a risk of Severe Hemolysis (red blood cell destruction) in individuals with a specific genetic condition, Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency. This serious reaction is classified as Very Rare.

Safety notes also identify particular populations that require caution:

  • Renal Impairment/Disease: Patients with existing kidney issues face an increased potential for stone formation and oxalate accumulation.
  • Geriatric and Pediatric Patients: Both older adults and children under two years old are noted as having a higher risk for oxalate nephropathy due to reduced or immature renal function.
  • Sodium Constraint: Because Celin contains sodium, use must be noted for patients on a sodium-restricted diet.

The overall regulatory structure emphasizes that while many adverse reactions are minor and systemic, the more clinically significant risks are closely linked to high-dose exposure over time and specific underlying patient risk factors, such as G6PD deficiency or hyperoxaluria.

Overdose and Emergency Response

The official regulatory profile for Celin (Sodium Ascorbate) overdose outlines documented manifestations, severe outcomes, and mandated emergency actions. Initial symptoms associated with intake exceeding two grams per day often affect the gastrointestinal system, including nausea, vomiting, abdominal cramps, and diarrhea, along with non-specific systemic effects such as headache, flushing, insomnia, or lethargy.

More serious outcomes documented in regulatory warnings are typically associated with massive or prolonged high doses. These life-threatening complications include the risk of oxalate nephropathy, the formation of renal oxalate calculi, and potential renal failure. Patients with pre-existing conditions, particularly renal disease or a history of oxalate kidney stones, are officially noted to face an increased risk of these severe effects. A specific risk of severe hemolysis is also documented for individuals with Glucose-6-phosphate dehydrogenase (G6PD) deficiency.

Immediate Emergency Actions

In the event of a suspected overdose, it is mandated that patients seek immediate medical attention. Urgent help is required for the development of severe clinical signs such as collapse, seizure, or difficulty breathing. The official guidance directs individuals to call the Poison Control Helpline for immediate advice. Management of overdose is primarily symptomatic and supportive treatment and may involve procedures like gastric lavage if ingestion was recent. Monitoring of renal function and blood count is necessary for high-risk patients.

Therapeutic Uses of Celin

Celin is commonly used across domains where additional symptomatic support is needed to address conditions presenting with systemic or localized discomfort. The information aligns with the therapeutic areas involving symptomatic relief for tissue health and general well-being.

Indications: The medication may be part of symptomatic management for conditions involving nutritional depletion, general weakness, issues with tissue health, and challenges to immune resilience. It is applied in scenarios where additional management of discomfort is required due to symptoms that create noticeable physiological strain.

“Supports the patient during difficult episodes by easing distress and assists with maintaining functional stability when symptoms are more noticeable.”

Core Therapeutic Benefits

The supportive relief provided by Celin helps address symptom clusters related to systemic imbalance, such as general weakness, and manifestations linked to affected tissue health, like poor wound healing or issues with gums. It is relevant when supportive symptom management is appropriate to support general well-being during symptomatic phases, and may assist with managing symptoms related to systemic imbalance where supportive assistance with iron is relevant. This provides support that may help patients cope more steadily with symptom fluctuations.


Quick Fact: Support for Symptoms of Fatigue and Weakness Celin is relevant for managing symptoms of fatigue related to nutritional status, helping improve day-to-day comfort during symptomatic periods.

Regulatory References

  1. NIH MedlinePlus overview of Vitamin C

Eligibility and Restrictions for Use

The eligibility profile for Celin, whose active substance is Sodium Ascorbate, is strictly determined by formal regulatory classifications for who can and cannot use the medicine.

Contraindicated Populations

Celin is strictly contraindicated in patients with a confirmed hypersensitivity to the active substance or to any component of the preparation. Use is also formally non-eligible for individuals diagnosed with hyperoxaluria (excessive oxalate excretion), as the medicine's metabolism increases the risk of oxalate accumulation. Furthermore, regulatory labels advise that patients with hemochromatosis or other forms of iron overload are typically restricted from high-dose use.

Restricted and Conditional Use

Use requires specific caution or is limited by dose in certain populations:

  • G6PD Deficiency: Patients with glucose-6-phosphate dehydrogenase deficiency are at risk of severe hemolysis, particularly with high doses, and should not exceed the U.S. Recommended Dietary Allowance (RDA).
  • Renal Risk: Individuals with severe renal impairment or a history of recurrent renal calculi (kidney stones) must use with caution due to the documented risk of oxalate nephropathy.
  • Age and Life Stage: Pregnancy and Lactation eligibility is established, but use is restricted to the RDA or doses needed to correct a deficiency. Infants under specific age thresholds may be deemed unsuitable for the specific product form.

What should I know about interactions with other medicines?

The official regulatory documentation identifies several interaction patterns for Celin (Sodium Ascorbate) with medicines and substances. A critical restriction involves Deferoxamine, where co-administration is strictly avoided in patients with cardiac failure due to the risk of worsening iron toxicity; furthermore, timing rules mandate that Celin supplementation must be delayed until after the first month of Deferoxamine therapy. Pharmacodynamic concerns are noted with Oral Anticoagulants, such as Warfarin, where high doses of ascorbic acid may reduce the expected therapeutic effect. The product is also documented to alter the systemic exposure of other compounds. It significantly increases the absorption of aluminum from aluminum-containing antacids, which is a key concern for patients with existing renal impairment. Separately, Celin can affect the plasma levels of certain basic drugs, including Amphetamines and Fluphenazine, by promoting urine acidification, thereby altering their renal clearance and decreasing their systemic exposure. The profile also highlights population-specific interaction cautions, noting an increased risk of severe hemolysis in patients with Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency when high doses are administered. Finally, official sources include substance interactions, documenting that alcohol and nicotine exposure is linked to inducing ascorbic acid tissue desaturation.

Mechanism of Action

How Celin Works: Mechanism of Action

The biological function of Sodium Ascorbate (Ascorbic Acid) is centered on its dual role as an essential enzyme cofactor and a core reducing agent in metabolic and cellular defense systems.


Enzyme Cofactor Activity

Ascorbic Acid sustains the catalytic activity of specific iron-dependent hydroxylase enzymes (like prolyl hydroxylase and lysyl hydroxylase) required for the Collagen Synthesis Pathway. The molecule donates electrons to maintain the enzyme's metal center in its necessary reduced state, ensuring the correct hydroxylation of amino acid residues. This process is necessary for forming the stable cross-links that establish the structural integrity of connective tissues, including blood vessel walls and bone matrix.

Systemic Redox Regulation

Ascorbic Acid acts as a non-enzymatic reducing agent and scavenger within the Antioxidant Defense System. By donating electrons, it directly neutralizes destructive Reactive Oxygen Species (ROS) and Reactive Nitrogen Species (RNS), arresting the propagation of the oxidative damage chain. This action results in the protection of cellular components and is instrumental in the maintenance of cellular homeostasis.


Neurotransmitter Pathway Support

In a separate action, the molecule functions as a cofactor for Dopamine beta-hydroxylase, an enzyme responsible for converting dopamine into the functional neurotransmitter norepinephrine. This facilitates the necessary endogenous production of catecholamines in the central and autonomic nervous systems.

Dosage and Administration Information

How Celin is Used: Official Administration Guidelines

Celin, which contains Sodium Ascorbate, is administered according to specific patterns that depend on its intended purpose, as defined by regulatory documents. The administration typically follows two distinct routes based on the patient's needs: Oral for routine supplementation and Parenteral (Intravenous, Intramuscular, or Subcutaneous) for acute or severe deficiency where oral absorption is compromised.


Administration Schedule and Dosage

Usage Context Daily Dosing Range Frequency Special Condition
Nutritional Supplementation (Oral) 50 mg to 200 mg Once daily Administered with food and water
Therapeutic Deficiency (Oral) 100 mg to 1,000 mg Once or twice daily Used for a minimum course duration
Acute Deficiency (IV/IM/SC) 300 mg to 1 gram Once daily Limited to a short-term course (e.g., 7 days)

Contextual Use and Preparation

When Celin is taken as an oral tablet for routine supplementation, the official guidance indicates it should be taken with food and a full glass of water. This approach is related to optimizing intake conditions and is a common procedural step for many oral preparations.

For parenteral administration, the injection solution is not to be administered directly. Regulatory protocols require the solution to be diluted in a compatible intravenous fluid prior to use, and it must be administered slowly as an infusion. Dosage adjustments for pediatric patients being treated for deficiency are also specified in the regulatory literature, typically prescribing lower milligram ranges in divided doses appropriate for the child's age.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Celin (Sodium Ascorbate)

The research landscape for Celin, which provides the essential nutrient Vitamin C as Sodium Ascorbate, focuses on correcting nutritional status and exploring its role in various conditions where supportive care is relevant. This overview summarizes the types of scientific evidence available from regulatory and high-quality peer-reviewed sources.


Evidence on Correcting and Preventing Vitamin C Deficiency

The research base for addressing the most severe form of deficiency, known as scurvy, relies primarily on historical evidence and modern clinical case reports. Studies explored the kinetics of the nutrient, focusing on how quickly plasma and white blood cell levels are raised and maintained. Studies report measurable changes in plasma and leukocyte vitamin C levels following administration of the nutrient, which reflects the nutrient's established biochemical function. However, deficiency is rare in the general population, meaning that large-scale randomized controlled trials for this specific endpoint are limited.


Studies of Celin for Adjunctive Support in Iron Status

The use of Vitamin C in combination with oral iron has been evaluated in randomized controlled trials (RCTs) and comprehensive meta-analyses. Research examined outcomes related to systemic or functional imbalance, specifically looking at changes in hematological markers like hemoglobin and ferritin in populations with Iron Deficiency Anemia. Findings were mixed across many of the trials and reviews. While some evidence suggests a measurable change in blood markers, other high-quality systematic reviews reported that findings related to outcomes like hemoglobin levels were often similar between the combination and iron-only groups.


Research Examining Respiratory Symptoms and Immune Function

A large body of evidence from multiple systematic reviews and meta-analyses has studied the patterns of regular Vitamin C supplementation on common respiratory symptoms. Studies monitored the duration and severity of the cold episode in those receiving regular supplementation and data show patterns related to the time it takes for symptoms to evolve. However, research exploring prevention was studied for an effect on the overall number of colds, but findings indicate that routine supplementation did not show a consistent pattern of reducing incidence in the general population.


Evidence Gaps and Research Uncertainty

Reviewers of the scientific literature note several key areas where certainty remains low or where further research is needed. A fundamental limitation is that many studies do not account for a person's baseline vitamin C status, which is known to influence the observed outcome dramatically. Additionally, long-term effects are not fully established, and subgroup findings are uncertain across many chronic conditions, meaning the results apply only to the populations studied and do not offer general conclusions.

Frequently Asked Questions (FAQ)

Common questions about Celin (FAQ)

Q: What is Celin, and what is it used for?

Celin is a brand name for the generic medicine ascorbic acid, also known as Vitamin C. It is primarily used to prevent or treat a condition called scurvy, which is caused by a severe deficiency of Vitamin C in the diet. Vitamin C is an essential nutrient needed by the body for the growth and repair of tissues, and it functions as an antioxidant.

Q: How should I take Celin?

Celin is available in several forms, including tablets, chewable tablets, and liquid. You should always follow the dosage instructions provided by your healthcare provider or as indicated on the product label. It can be taken with or without food. If you are using a chewable tablet, chew it thoroughly before swallowing. If you are using the liquid form, measure the dose carefully using the provided measuring device to ensure accuracy.

Q: What are the common side effects of Celin?

When taken at recommended doses, Celin is generally well-tolerated and side effects are uncommon. However, at higher doses, some people may experience gastrointestinal side effects, such as stomach cramps, nausea, diarrhea, and heartburn. Rarely, high doses may also be associated with the formation of kidney stones. If you experience severe or persistent side effects, you should consult your healthcare provider.

Q: Can I take Celin with other vitamins or supplements?

Generally, Celin (Vitamin C) is safe to take with most other vitamins and supplements. However, it is important to tell your healthcare provider about all the products you use, including vitamins, over-the-counter medicines, and herbal supplements, to check for any potential interactions. Vitamin C can sometimes affect the absorption or metabolism of other substances, such as iron.

Q: What should I do if I miss a dose?

If you miss a dose of Celin, take it as soon as you remember. If it is almost time for your next scheduled dose, skip the missed dose and continue with your regular dosing schedule. Do not take two doses at the same time to make up for a missed dose.

How should Celin be stored and disposed of?

How to Store and Dispose of Celin (Sodium Ascorbate)

Celin must be stored according to regulatory requirements to protect the product from degradation, as Ascorbic Acid is sensitive to environmental factors.

Storage Requirements

Condition Requirement
Temperature Store below 30 C (86 F).
Protection Protect from light and moisture. Store in a cool and dry place.
Handling Note Avoid contact with metals.
Child Safety Keep out of the sight and reach of children.

Although Celin Tablets may show slight darkening over time, the medicinal value remains unchanged.

Disposal

Disposal of unused or expired Celin should follow official regulatory guidance, prioritizing drug take-back programs. If a take-back option is unavailable, the medicine can be prepared for household trash by mixing it with an undesirable substance (e.g., dirt) and sealing it in a container before discarding.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

Available in countries:

Equivalent of Celin found in:

A-Z Index: