Verifying…
Home / Drug A–Z / Mazimed Infant Mucus Extractor

Mazimed Infant Mucus Extractor

NAFDAC Reg. No. A3-101306 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Mazimed Infant Mucus Extractor
NAFDAC number
A3-101306
Active ingredient
Mucus Extractor
Strength
NA
Form
NA
Pack size
25 pieces (in PVC pouch)
Manufacturer
Not listed
Applicant (holder)
Okeymazi Pharmaceutical Limited
Approved
1 Aug 2024
Status
Active View on NAFDAC ↗
Registration valid to
30 Jul 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Mazimed Infant Mucus Extractor is on the NAFDAC register with an active registration (A3-101306). 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 Mazimed Infant Mucus Extractor

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

25% Dextrose Injection is indicated in the treatment of acute symptomatic episodes of hypoglycemia in the neonate or older infant to restore depressed blood glucose levels and control symptoms. Other drugs, such as epinephrine and glucagon, should be considered in patients unresponsive or intolerant to dextrose (glucose). Oral feeding of dextrose may be necessary in infants with frequently recurring hypoglycemic episodes or to prevent recurrences due to hyperinsulinemia. 25% Dextrose Injection also provides a minimal source of carbohydrate calories.

How to take it and how often
  • When possible, glucose concentrations of greater than 12% should be administered by central vein to reduce the risk for phlebitis and thrombosis. 25% Dextrose Injection, USP is administered only by slow intravenous injection
  • The dosage and constant infusion rate of intravenous dextrose must be selected with caution, particularly in
  • Neonates and low birth weight
  • Infants, because of the increased risk of hyperglycemia/ hypoglycemia
  • In the neonate, an injection of 250 to 500 mg (1 to 2 mL)/kg/dose (5 to 10 mL of 25% dextrose in a 5 kg infant) is recommended to control acute symptomatic hypoglycemia (tremors, convulsions, etc.)
  • Larger or repeated single doses (up to 10 or 12 mL of 25% dextrose) may be required in severe cases or older
  • Infants
  • A specimen for blood glucose determination should be taken before injecting the dextrose
  • In such emergencies, dextrose should be administered promptly without awaiting pretreatment test results
  • Subsequent continuous intravenous infusion of 10% dextrose injection may be needed to stabilize blood glucose levels
  • Further treatment should be guided by evaluation of the underlying disorder
  • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. (See PRECAUTIONS )
Talk to a doctor first if

A concentrated dextrose solution should not be used when intracranial or intraspinal hemorrhage is present.

Warnings

25% Dextrose Injection, USP is hypertonic and may cause phlebitis and thrombosis at the site of injection. Significant hyperglycemia and possible hyperosmolar syndrome may result from too rapid administration. The physician should be aware of the symptoms of hyperosmolar syndrome, such as loss of consciousness.

Possible side effects

Hyperosmolar syndrome, resulting from excessively rapid administration of concentrated dextrose may cause mental confusion and/or loss of consciousness. Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection and extravasation. If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures, and save the remainder of the fluid for examination if deemed necessary.

If you take too much

In the event of overdosage (hyperglycemia) during therapy, re-evaluate the patient and institute appropriate corrective measures. (See WARNINGS and PRECAUTIONS .)

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

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 2022-12-09.

Label for Mazimed Infant Mucus Extractor, the active ingredient registered with NAFDAC.

Check your pack of Mazimed Infant Mucus Extractor

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Mazimed Infant Mucus Extractor

What is in Mazimed Infant Mucus Extractor?

Mazimed Infant Mucus Extractor contains Mucus Extractor (NA), as na, according to its NAFDAC registration record.

Is Mazimed Infant Mucus Extractor registered with NAFDAC?

Yes. Mazimed Infant Mucus Extractor is listed on the NAFDAC register under registration number A3-101306, and its registration is active as of 28 October 2026.

Has Mazimed Infant Mucus Extractor been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Mazimed Infant Mucus Extractor in our automatically synced alert list.

How can I check that my pack of Mazimed Infant Mucus Extractor is genuine?

Run a free authenticity scan with the NAFDAC number A3-101306, 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 Mazimed Infant Mucus Extractor?

Follow your prescription or the leaflet in your pack. The official label says: When possible, glucose concentrations of greater than 12% should be administered by central vein to reduce the risk for phlebitis and thrombosis. 25% Dextrose Injection, USP is administered only by slow intravenous injection. The dosage and constant infusion rate of intravenous dextrose must be selected with caution, particularly in neonates and low birth weight infants, becaus…

What is Mazimed Infant Mucus Extractor used for?

25% Dextrose Injection is indicated in the treatment of acute symptomatic episodes of hypoglycemia in the neonate or older infant to restore depressed blood glucose levels and control symptoms. Other drugs, such as epinephrine and glucagon, should be considered in patients unresponsive or intolerant to dextrose (glucose). Oral feeding of dextrose may be necessary in infants with frequently recurri (Summarised from the official U.S. FDA label for Mazimed Infant Mucus Extractor. Always follow your doctor or pharmacist.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Mazimed Infant Mucus Extractor? Share your experience to help other patients. Sign in to review

Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.