all day pain relief

Generic: naproxen sodium

Labeler: walmart inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day pain relief
Generic Name naproxen sodium
Labeler walmart inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Walmart Inc.

Identifiers & Regulatory

Product NDC 79903-389
Product ID 79903-389_34ae94cb-6d62-c8f2-e063-6394a90aa297
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA090545
Listing Expiration 2026-12-31
Marketing Start 2025-05-10

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79903389
Hyphenated Format 79903-389

Supplemental Identifiers

RxCUI
849574
UPC
0194346497980
UNII
9TN87S3A3C

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name all day pain relief (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA090545 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (79903-389-50) / 50 TABLET in 1 BOTTLE
source: ndc

Packages (1)

79903-389-50 1 BOTTLE in 1 CARTON (79903-389-50) / 50 TABLET in 1 BOTTLE

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

All Day Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34ae94cb-6d62-c8f2-e063-6394a90aa297", "openfda": {"upc": ["0194346497980"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["32df7378-4dd1-4f7e-e063-6394a90ad948"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-389-50)  / 50 TABLET in 1 BOTTLE", "package_ndc": "79903-389-50", "marketing_start_date": "20250510"}], "brand_name": "All Day Pain Relief", "product_id": "79903-389_34ae94cb-6d62-c8f2-e063-6394a90aa297", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-389", "generic_name": "Naproxen Sodium", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20250510", "listing_expiration_date": "20261231"}