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Min-C Drops

NAFDAC Reg. No. B4-1983 · Drug

Registered with NAFDAC. Registration activeAs of 29 October 2026 · synced automatically from official sources.
Product
Min-C Drops
رقم NAFDAC
B4-1983
المادة الفعالة
Ascorbic Acid
التركيز
100 mg/mL
الشكل
Drops
حجم العبوة
1 x 15 mL (in amber glass bottle)
Manufacturer
Not listed
Applicant (holder)
Ugo Lab Productions (Nig). Ltd
Approved
21 Dec 2023
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
20 Dec 2028
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

About the medicine: Ascorbic acid: uses, dosage and brands worldwide

What we found

  • Min-C Drops is on the NAFDAC register with an active registration (B4-1983). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Min-C Drops

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

Ascorbic acid injection is indicated for the short term (up to 1 week) treatment of scurvy in adult and pediatric patients, age 5 months and older, for whom oral administration is not possible, insufficient or contraindicated. Limitations of Use Ascorbic acid injection is not indicated for the treatment of vitamin C deficiency that is not associated with signs and symptoms of scurvy. Ascorbic acid injection is vitamin C indicated for the short term (up to 1 week) treatment of scurvy in adult and pediatric patients age 5 months and older for whom oral administration is not possible, insufficient or contraindicated. …

كيف يُتناول وكم مرة
  • Supplied in a Pharmacy Bulk Package (PBP)
  • Dispense single doses to multiple patients in a pharmacy admixture program; use within 4 hours of puncture. • Must be diluted prior to use • Administer as a slow intravenous infusion • See Full Prescribing Information for important administration instructions • Maximum recommended duration is one week Population Recommended Doses
  • Pediatric patients age 5 months to less than 12 months 50 mg once daily
  • Pediatric patients age 1 year to less than 11 years 100 mg once daily
  • Adults and pediatric patients age 11 years and older 200 mg once daily Specific Populations Pregnant women, lactating women, patients with glucose-6-phosphate dehydrogenase deficiency Should not exceed the U.S
  • Recommended Dietary Allowance (RDA) Important Preparation and Administration Instructions • Ascorbic acid injection vials contain 25,000 mg of ascorbic acid and the largest recommended single dose is 200 mg
  • Do not give the entire contents of the vial to a single patient. • Do not administer ascorbic acid injection as an undiluted intravenous injection. • Minimize exposure to light because ascorbic acid injection is light sensitive. • Ascorbic acid injection is supplied as a Pharmacy Bulk Package (PBP) which is intended for dispensing of single doses to multiple patients in a pharmacy admixture program and is restricted to the preparation of admixtures for infusion: a. Use only in a suitable ISO Class 5 work area such as a laminar flow hood (or an equivalent clean air compounding area). …
Strengths it comes in

Injection: 25,000 mg per 50 mL (500 mg per mL) supplied as a Pharmacy Bulk Package (colorless to pale yellow solution) Injection: 25,000 mg per 50 mL (500 mg per mL) - Pharmacy Bulk Package

Children
  • Ascorbic acid injection is indicated for the short term (up to 1 week) treatment of scurvy
  • In pediatric patients age 5 months and older for whom oral administration is not possible, insufficient or contraindicated
  • The safety profile of ascorbic acid
  • In pediatric patients is similar to adults; however, pediatric patients less than 2 years of age may be at higher risk of oxalate nephropathy following ascorbic acid administration due to age-related decreased glomerular filtration [see Warnings and Precautions ]. …
Older adults

Glomerular filtration rate is known to decrease with age and as such may increase risk for oxalate nephropathy following ascorbic acid administration in elderly population [see Warnings and Precautions (5.1) ] .

While you are taking it
  • Inform patients that treatment with ascorbic acid injection may increase their risk of oxalate nephropathy [see Warnings and Precautions ]. • Inform patients that treatment with ascorbic acid injection may impact laboratory results, including blood and urine glucose tests, up to 24 hours after infusion [see Warnings and Precautions ]. • Inform patients with glucose-6-phosphate dehydrogenase deficiency that treatment with ascorbic acid injection may increase their risk of hemolysis [see Warnings and Precautions ]
  • Manufactured by: Lake Zurich, IL 60047 www.fresenius-kabi.com/us 451857 Fresenius Kabi Logo
Talk to a doctor first if
  • None
  • None
Medicines it may not mix with

• Antibiotics: Ascorbic acid may decrease the activities of erythromycin, kanamycin, streptomycin, doxycycline, and lincomycin. Bleomycin is inactivated in vitro by ascorbic acid ( 7.1 ). • Amphetamine and Other Drugs Affected by Urine Acidification: Ascorbic acid may cause acidification of the urine and result in decreased amphetamine serum levels and affect excretion and plasma concentrations of other drugs sensitive to urine pH ( 7.2 ). • Warfarin: Continue standard monitoring ( 7.3 ). 7.1 Antibiotics Ascorbic acid may decrease activities of erythromycin, kanamycin, streptomycin, doxycycline, and lincomycin. Bleomycin is inactivated in vitro by ascorbic acid. …

Warnings

• Oxalate nephropathy and Nephrolithiasis : Ascorbic acid has been associated with development of acute or chronic oxalate nephropathy following prolonged use of high doses of ascorbic acid infusion. Patients with renal disease including renal impairment, history of oxalate kidney stones, geriatric patients, and pediatric patients less than 2 years old may be at increased risk ( 5.1 ). • Hemolysis : Patients with glucose-6-phosphate dehydrogenase deficiency are at risk of severe hemolysis; a reduced dose is recommended ( 5.2 ). …

الآثار الجانبية المحتملة

The following adverse reactions are discussed in greater detail in other sections of the labeling: • Oxalate nephropathy and Nephrolithiasis [see Warnings and Precautions (5.1) ]. • Hemolysis in patients with glucose-6-phosphate dehydrogenase deficiency [see Warnings and Precautions (5.2) ]. The following adverse reactions associated with the use of ascorbic acid were identified in the literature. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency reliably or to establish a causal relationship to drug exposure: Administration site reactions: pain and swelling. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary There are no available data on use of ascorbic acid injection in pregnant women to inform a drug-associated risk of adverse developmental outcomes; however, use of ascorbic acid (vitamin C) has been used during pregnancy for several decades and no adverse developmental outcomes are reported in the published literature [see Data]. …

If you take too much

Overdose with ascorbic acid may cause nausea, vomiting, diarrhea, facial flushing, rash, headache, fatigue or disturbed sleep. If overdose of ascorbic acid injection occurs, immediately discontinue administration and treat symptoms and signs of overdose, avoiding additional intake of ascorbic acid.

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-12-17.

Label for ascorbic acid, the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No.019/2026 – Alert on Mop up of all Otrivin Nasal Drops (0.05% and 0.1%)14 Mar 2026 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is alerting healthcare providers and the public about a report concerning the circulation of counterfeit and unregistered Otrivin Nasal drops (0.05%) for children and (0.01%) for adults in Nigeria.The Post Marketing Surveillance (PMS) Directorate…Public Alert No. 035/2023 -Alert on Recall One lot of Growlyn Drops 50 ml in Abu Dhabi1 Nov 2023 · nafdac.gov.ngThe National Agency for Food and Drugs Administration and Control (NAFDAC) is notifying the public that the United Arab Emirate Ministry of Health and Prevention (MOHAP) in Abu Dhabi issued a safety recall on Growlyn Drops 50ml manufactured by Aeon Formulations Pvt. Ltd., India. Laboratory analysis conducted on the pro…Public Alert No:008/2023 – Alert on Recalled artificial tears eye drops linked to death, blindness and eyeball removals in US22 Mar 2023 · nafdac.gov.ng, The National Agency for Food and Drugs Administration and Control (NAFDAC) is notifying the public that Global Pharma Healthcare have recalled EzriCare and Delsam Pharma Artificial Tears eye drops early in February. The recall of the preservative-free eye drops were due to suspected contamination with pseudomonas aer…Public Alert No. 006/2022- Public Alert On Class 2 Recall Of IKERVIS 1MG/ML Eye Drops, Emulsion10 Feb 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) is notifying healthcare providers that Medicines & Healthcare products Regulatory Agency (MHRA) and the Health Science Authority Singapore is recalling one lot each of IKERVIS 1 mg/mL eye drops manufactured by SANTEN Oy (trading as Santen UK Li…

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

Check your pack of Min-C Drops

Add the expiry date on your pack for a full Trust Score.

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم المصادر الرسمية: FDA الأمريكية · EMA (الاتحاد الأوروبي) · NAFDAC · تنبيهات منظمة الصحة العالمية

About Min-C Drops

What is in Min-C Drops?

Min-C Drops contains Ascorbic Acid (100 mg/mL), as drops, according to its NAFDAC registration record.

Is Min-C Drops registered with NAFDAC?

Yes. Min-C Drops is listed on the NAFDAC register under registration number B4-1983, and its registration is active as of 29 October 2026.

Has Min-C Drops been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Min-C Drops in our automatically synced alert list.

How can I check that my pack of Min-C Drops is genuine?

Run a free authenticity scan with the NAFDAC number B4-1983, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Min-C Drops?

Follow your prescription or the leaflet in your pack. The official label says: • Supplied in a Pharmacy Bulk Package (PBP). Dispense single doses to multiple patients in a pharmacy admixture program; use within 4 hours of puncture. ( 2.1 ) • Must be diluted prior to use ( 2.1 ) • Administer as a slow intravenous infusion ( 2.1 ) • See Full Prescribing Information for important administration instructions ( 2.1 ) • Maximum recommended duration is one week …

What is Min-C Drops used for?

Ascorbic acid injection is indicated for the short term (up to 1 week) treatment of scurvy in adult and pediatric patients, age 5 months and older, for whom oral administration is not possible, insufficient or contraindicated. Limitations of Use Ascorbic acid injection is not indicated for the treatment of vitamin C deficiency that is not associated with signs and symptoms of scurvy. Ascorbic acid (Summarised from the official U.S. FDA label for ascorbic acid. Always follow your doctor or pharmacist.)

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