All Day Back and Muscle Pain Relief

Generic: Naproxen Sodium

Labeler: WALMART INC.
NDC Directory HUMAN OTC DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name All Day Back and Muscle Pain Relief
Generic Name Naproxen Sodium
Labeler WALMART INC.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

NAPROXEN SODIUM 220 mg/1

Identifiers & Regulatory

Product NDC 79903-098
Product ID 79903-098_92579484-1eab-438a-8079-984015a1dd9f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204872
Marketing Start 2022-01-17
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79903098
Hyphenated Format 79903-098

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 ANDA204872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (79903-098-06) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (79903-098-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

79903-098-06 1 BOTTLE, PLASTIC in 1 CARTON (79903-098-06) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 79903-098-52 1 BOTTLE, PLASTIC in 1 CARTON (79903-098-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

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": "92579484-1eab-438a-8079-984015a1dd9f", "openfda": {"upc": ["0681131071307"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["b54250d5-edcc-450a-9b87-d7bdb5fc301b"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (79903-098-06)  / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "79903-098-06", "marketing_end_date": "20260228", "marketing_start_date": "20220117"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (79903-098-52)  / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "79903-098-52", "marketing_end_date": "20260228", "marketing_start_date": "20220117"}], "brand_name": "All Day Back and Muscle Pain Relief", "product_id": "79903-098_92579484-1eab-438a-8079-984015a1dd9f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-098", "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": "ANDA204872", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20220117"}