all day pain relief

Generic: naproxen sodium

Labeler: walgreens
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

naproxen sodium 220 mg/1

Manufacturer
WALGREENS

Identifiers & Regulatory

Product NDC 0363-6099
Product ID 0363-6099_13b172b6-b829-8fe5-e063-6294a90a37e3
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA090545
Listing Expiration 2026-12-31
Marketing Start 2019-06-30

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 03636099
Hyphenated Format 0363-6099

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 ANDA090545 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (0363-6099-01)
  • 50 TABLET, COATED in 1 BOTTLE (0363-6099-05)
  • 200 TABLET, COATED in 1 BOTTLE (0363-6099-20)
source: ndc

Packages (3)

0363-6099-01 100 TABLET, COATED in 1 BOTTLE (0363-6099-01) 0363-6099-05 50 TABLET, COATED in 1 BOTTLE (0363-6099-05) 0363-6099-20 200 TABLET, COATED in 1 BOTTLE (0363-6099-20)

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": "13b172b6-b829-8fe5-e063-6294a90a37e3", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["8771300f-e907-3d53-e053-2a95a90ae402"], "manufacturer_name": ["WALGREENS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (0363-6099-01)", "package_ndc": "0363-6099-01", "marketing_start_date": "20190708"}, {"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (0363-6099-05)", "package_ndc": "0363-6099-05", "marketing_start_date": "20190708"}, {"sample": false, "description": "200 TABLET, COATED in 1 BOTTLE (0363-6099-20)", "package_ndc": "0363-6099-20", "marketing_start_date": "20190708"}], "brand_name": "ALL DAY PAIN RELIEF", "product_id": "0363-6099_13b172b6-b829-8fe5-e063-6294a90a37e3", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-6099", "generic_name": "NAPROXEN SODIUM", "labeler_name": "WALGREENS", "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": "20190630", "listing_expiration_date": "20261231"}