United States · FDA National Drug Code directory
All Day Back and Muscle 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
- 79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fc
- Product NDC
- 79903-609
- Form
- TABLET, COATED
- Composition / generic term
- Naproxen sodium
- Labeler
- Walmart Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231215
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN SODIUM — 220 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE · 79903-609-09
- 1 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLE · 79903-609-20
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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