all day pain relief

Generic: naproxen sodium

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day pain relief
Generic Name naproxen sodium
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0368
Product ID 0363-0368_889efbbf-10a8-4b8b-b9cb-d8eca7b839c7
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 1997-01-14

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 03630368
Hyphenated Format 0363-0368

Supplemental Identifiers

RxCUI
849574
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 ANDA074661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-0368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-0368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-0368-76) / 120 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

0363-0368-71 1 BOTTLE in 1 CARTON (0363-0368-71) / 50 TABLET, FILM COATED in 1 BOTTLE 0363-0368-75 1 BOTTLE in 1 CARTON (0363-0368-75) / 90 TABLET, FILM COATED in 1 BOTTLE 0363-0368-76 1 BOTTLE in 1 CARTON (0363-0368-76) / 120 TABLET, FILM COATED 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": "889efbbf-10a8-4b8b-b9cb-d8eca7b839c7", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["318d4e2a-7108-4e88-8e56-5bec17ca4a3e"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0368-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-0368-71", "marketing_start_date": "19970114"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0368-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-0368-75", "marketing_start_date": "20220726"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0368-76)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-0368-76", "marketing_start_date": "20020711"}], "brand_name": "All Day Pain Relief", "product_id": "0363-0368_889efbbf-10a8-4b8b-b9cb-d8eca7b839c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-0368", "generic_name": "Naproxen Sodium", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "19970114", "listing_expiration_date": "20261231"}