United States · FDA National Drug Code directory
All Day Pain Relief
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84b
- Product NDC
- 69517-109
- Form
- TABLET
- Composition / generic term
- Naproxen Sodium Tablets, 220 mg
- Labeler
- HealthLife of USA LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110930
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN SODIUM — 220 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCH · 69517-109-02
- 400 BOTTLE in 1 BOTTLE (69517-109-04) / 100 BOTTLE in 1 BOTTLE (69517-109-01) / 24 CARTON in 1 BOTTLE (69517-109-24) / 1 TABLET in 1 CARTON · 69517-109-04
- 25 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCH · 69517-109-25
- 50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCH · 69517-109-50
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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