Pain Relief Acetaminophen PM Extra Strength
Active substance: ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE
TABLET, FILM COATED · ACETAMINOPHEN 500 mg/1, DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
United StatesActive
Marketing holder: Rite Aid Corporation
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
Composition
- ACETAMINOPHEN · 500 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE · 25 mg/1
Registration
- Registration number
- 11822-2350
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 11822-2350 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 11822-2350 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 11822-2350 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 11822-2350 · Verified 2026-10-09 · open in source