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Drujela Mouth Gel

NAFDAC Reg. No. 04-8492 · Drug

Registered with NAFDAC. Registration activeAs of 4 November 2026 · synced automatically from official sources.
Product
Drujela Mouth Gel
NAFDAC number
04-8492
Active ingredient
Choline Salicylate; Cetalkonium Chloride
Strength
8.7%; 0.01%
Form
Dental gel
Pack size
1 x 10 g (in a tube)
Manufacturer
Not listed
Applicant (holder)
Drugfield Pharmaceuticals Limited
Approved
28 Sep 2023
Status
Active View on NAFDAC ↗
Registration valid to
27 Sep 2028
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Choline salicylate: uses, dosage and brands worldwide

What we found

  • Drujela Mouth Gel is on the NAFDAC register with an active registration (04-8492). 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 Drujela Mouth 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

Temporarily relieves minor aches and pains due to: ○ headache ○ minor arthritis pain ○ muscle aches ○ menstrual cramps ○ backache temporarily reduces fever

How to take it and how often
  • Do not take more than directed
  • Adults and children 12 years of age and over: take 30mL every 6 hours, while symptoms persist do not take exceed 4 doses in any 24 hours unless directed by a doctor
  • Children under 12 years of age: ask a doctor use enclosed dose cup
While you are taking it
  • Limit the use of caffeine-containing medications, foods, or beverages because too much caffeine may cause nervousness, irritability, sleeplessness, and occasionally, rapid heart beat the recommended dose of this product contains about as much caffeine as a cup of coffee
  • Take with food or milk if stomach upset occurs
Talk to a doctor first if

Ask a doctor before use if stomach bleeding warning applies to you you have high blood pressure, heart disease, liver cirrhosis, or kidney disease you are taking a diuretic you have a history of stomach problems such as heartburn, upset stomach, stomach pain, or ulcers you have asthma

Warnings

Reye's syndrome Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness. Allergy alert Salicylates (NSAIDs) may cause a severe allergic reaction which may include: hives skin reddening rash facial swelling shock asthma (wheezing) Stomach bleeding warning This product contains an NSAID, which may cause severe stomach bleeding. …

Possible side effects

An allergic reaction occurs. Seek medical help right away. you experience any of the following signs of stomach bleeding: ○ feel faint ○ vomit blood ○ have bloody or black stools ○ have stomach pain that does not get better symptoms do not improve pain gets worse or lasts more than 10 days ringing in the ears or loss of hearing occurs redness or swelling is present new symptoms occur fever gets worse or lasts more than 3 days

How to store it

Keep out of reach of children.

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 2025-10-15.

Label for choline salicylate and cetalkonium chloride, the active ingredient registered with NAFDAC.

Check your pack of Drujela Mouth 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 Drujela Mouth Gel

What is in Drujela Mouth Gel?

Drujela Mouth Gel contains Choline Salicylate; Cetalkonium Chloride (8.7%; 0.01%), as dental gel, according to its NAFDAC registration record.

Is Drujela Mouth Gel registered with NAFDAC?

Yes. Drujela Mouth Gel is listed on the NAFDAC register under registration number 04-8492, and its registration is active as of 4 November 2026.

Has Drujela Mouth Gel been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Drujela Mouth Gel in our automatically synced alert list.

How can I check that my pack of Drujela Mouth Gel is genuine?

Run a free authenticity scan with the NAFDAC number 04-8492, 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 Drujela Mouth Gel?

Follow your prescription or the leaflet in your pack. The official label says: do not take more than directed. adults and children 12 years of age and over: take 30mL every 6 hours, while symptoms persist do not take exceed 4 doses in any 24 hours unless directed by a doctor children under 12 years of age: ask a doctor use enclosed dose cup…

What is Drujela Mouth Gel used for?

temporarily relieves minor aches and pains due to: ○ headache ○ minor arthritis pain ○ muscle aches ○ menstrual cramps ○ backache temporarily reduces fever (Summarised from the official U.S. FDA label for choline salicylate and cetalkonium chloride. 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.