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Predlife Tablets

NAFDAC Reg. No. B4-7603 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Predlife Tablets
NAFDAC number
B4-7603
Active ingredient
Prednisolone
Strength
5 mg
Form
Tablet
Pack size
10 x 10's (in Alu-PVC blisters)
Manufacturer
Not listed
Applicant (holder)
Life - Line Pharmaceuticals Ltd
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

What we found

  • Predlife Tablets is on the NAFDAC register with an active registration (B4-7603). 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 Predlife Tablets

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 protects minor: cuts, scrapes, burns. temporarily protects and helps relieve chapped or cracked skin and lips. helps protect from the drying effects of wind and cold weather.

How to take it and how often

Apply as needed.

While you are taking it

Do not get in eyes.

Talk to a doctor first if

on Deep or puncture wounds animal bites. serious burns

Warnings

For external use only When using this product Do not get in eyes. Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur within a few days. Do not use on Deep or puncture wounds animal bites. serious burns Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Possible side effects

condition worsens symptoms last more than 7 days or clear up and occur within a few 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 2026-05-03.

Label for Predlife Tablets, the active ingredient registered with NAFDAC.

Check your pack of Predlife Tablets

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 Predlife Tablets

What is in Predlife Tablets?

Predlife Tablets contains Prednisolone (5 mg), as tablet, according to its NAFDAC registration record.

Is Predlife Tablets registered with NAFDAC?

Yes. Predlife Tablets is listed on the NAFDAC register under registration number B4-7603, and its registration is active as of 28 October 2026.

Has Predlife Tablets been flagged as fake or recalled?

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

How can I check that my pack of Predlife Tablets is genuine?

Run a free authenticity scan with the NAFDAC number B4-7603, 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 Predlife Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Apply as needed.…

What is Predlife Tablets used for?

temporarily protects minor: cuts, scrapes, burns. temporarily protects and helps relieve chapped or cracked skin and lips. helps protect from the drying effects of wind and cold weather. (Summarised from the official U.S. FDA label for Predlife Tablets. 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.