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.
From the official U.S. FDA label for benzyl benzoate, the active ingredient registered with NAFDAC.
Temporary Pain Relief
Topical Anasthetic Purpose Topical Anesthetic
Skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering Conditions worsen Symptoms persist for more than 7 days Symptoms clear up and occur again within a few days
On wounds or damaged skin In large quantities With a heating pad if you are allergic to any ingredients of this product
For external Use Only Do not use in eyes in large quantities over raw or blistered areas, or on deep puncture wounds, animal bites, or serious burns for more than one week unless directed by a doctor
If Pregnant or Breast Feeding Ask a health professional before use
Add the expiry date on your pack for a full Trust Score.
Bebe Lotion contains Benzyl Benzoate (25%), as lotion, according to its NAFDAC registration record.
Yes. Bebe Lotion is listed on the NAFDAC register under registration number 04-5917, and its registration is active as of 27 October 2026.
No WHO falsified or substandard medical product alert currently matches Bebe Lotion in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number 04-5917, 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.
Temporary Pain Relief (Summarised from the official U.S. FDA label for benzyl benzoate. Always follow your doctor or pharmacist.)
Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.