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Praicon Gel_

NAFDAC注册号 A4-101437 药物

已在NAFDAC注册。注册有效As of 5 November 2026 · synced automatically from official sources.
产品
Praicon Gel_
NAFDAC编号
A4-101437
活性成分
Silicon Dioxide
强度
10 mg
年级
Gel
包装规格
1 x 15 g (in tube)
制造商
未上榜
申请人(持有人)
Praipec Pharmaceutical Ltd
Approved
30 Jul 2025
Status
Active View on NAFDAC ↗
Registration valid to
29 Jul 2030
WHO提醒
None found
Community reports
None
Times checked
0

About the medicine: Silicon dioxide: uses, dosage and brands worldwide

What we found

  • Praicon Gel_ is on the NAFDAC register with an active registration (A4-101437). 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 Praicon Gel_

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

Condition listed above or as directed by a physician.

How to take it and how often

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Talk to a doctor first if

if pellet-dispenser seal is broken.

Warnings

Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

Pregnancy and breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

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 2024-01-30.

Label for silicon dioxide, the active ingredient registered with NAFDAC.

Check your pack of Praicon Gel_

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Praicon Gel_

What is in Praicon Gel_?

Praicon Gel_ contains Silicon Dioxide (10 mg), as gel, according to its NAFDAC registration record.

Is Praicon Gel_ registered with NAFDAC?

Yes. Praicon Gel_ is listed on the NAFDAC register under registration number A4-101437, and its registration is active as of 5 November 2026.

Has Praicon Gel_ been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Praicon Gel_ in our automatically synced alert list.

How can I check that my pack of Praicon Gel_ is genuine?

Run a free authenticity scan with the NAFDAC number A4-101437, 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 Praicon Gel_?

Follow your prescription or the leaflet in your pack. The official label says: (adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.…

What is Praicon Gel_ used for?

Condition listed above or as directed by a physician. (Summarised from the official U.S. FDA label for silicon dioxide. Always follow your doctor or pharmacist.)

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