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 medical device, the active ingredient registered with NAFDAC.
for relief of occasional constipation (irregularity). Generally produces bowel movement in 1/2 to 6 hours
Saline Laxtive
you have rectal bleeding or failure to have a bowel movement after use. These could be signs of a serious condition.
kidney disease a magnesium restricted diet abdorominal pain, nausea, or vomiting noticed a sudden change in bowel habits that persists over a period of 2 weeks already used a laxative for a period longer than 1 week
IF PREGNANT OR BREAST-FEEDING ask health professional before use.
Add the expiry date on your pack for a full Trust Score.
Lady Lili Ultra Soft and Gentle Ultra - Lite (Extra Long) contains Medical device (NA), as na, according to its NAFDAC registration record.
Yes. Lady Lili Ultra Soft and Gentle Ultra - Lite (Extra Long) is listed on the NAFDAC register under registration number A3-100376, and its registration is active as of 27 October 2026.
No WHO falsified or substandard medical product alert currently matches Lady Lili Ultra Soft and Gentle Ultra - Lite (Extra Long) in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A3-100376, 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.
for relief of occasional constipation (irregularity). Generally produces bowel movement in 1/2 to 6 hours (Summarised from the official U.S. FDA label for medical device. 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.