ALL NIGHT PAIN RELIEF PM
Active substance: DIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUM
TABLET, FILM COATED · DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1, NAPROXEN SODIUM 220 mg/1
United StatesActive
Marketing holder: Walgreen Company
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
Composition
- DIPHENHYDRAMINE HYDROCHLORIDE · 25 mg/1
- NAPROXEN SODIUM · 220 mg/1
Products containing diphenhydramine in other countries
Showing products with this active substance, combinations included; the full composition is shown for each product.
| Country | Products |
|---|---|
| RU 73 |
|
Registration
- Registration number
- 0363-2264
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 0363-2264 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 0363-2264 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 0363-2264 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 0363-2264 · Verified 2026-10-09 · open in source