all day back and muscle pain relief

Generic: naproxen sodium

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

Drug Facts

Product Profile

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

naproxen sodium 220 mg/1

Manufacturer
Walmart Inc.

Identifiers & Regulatory

Product NDC 79903-609
Product ID 79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fc
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA090545
Listing Expiration 2026-12-31
Marketing Start 2023-12-15

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 79903609
Hyphenated Format 79903-609

Supplemental Identifiers

RxCUI
849574
UPC
0194346189106 0194346189113
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 back and muscle 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 (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (2)

79903-609-09 1 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE 79903-609-20 1 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLE

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

All Day Back and Muscle Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0bafa4ac-8c2d-006b-e063-6294a90ab1fc", "openfda": {"upc": ["0194346189106", "0194346189113"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["062b9ffe-b4fc-9f5a-e063-6294a90a560e"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-609-09)  / 90 TABLET, COATED in 1 BOTTLE", "package_ndc": "79903-609-09", "marketing_start_date": "20231215"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-609-20)  / 200 TABLET, COATED in 1 BOTTLE", "package_ndc": "79903-609-20", "marketing_start_date": "20231215"}], "brand_name": "All Day Back and Muscle Pain Relief", "product_id": "79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fc", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-609", "generic_name": "Naproxen sodium", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Back and Muscle Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}