all day pain relief

Generic: naproxen sodium

Labeler: zapotol products corp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

naproxen sodium 220 mg/1

Manufacturer
Zapotol Products Corp

Identifiers & Regulatory

Product NDC 59428-604
Product ID 59428-604_9d429a1c-a5e0-4739-80a5-d3c39ef7a764
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204872
Listing Expiration 2026-12-31
Marketing Start 2020-10-22

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 59428604
Hyphenated Format 59428-604

Supplemental Identifiers

RxCUI
849574
UPC
0647755015004
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 ANDA204872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (59428-604-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

59428-604-08 1 BOTTLE, PLASTIC in 1 CARTON (59428-604-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

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": "9d429a1c-a5e0-4739-80a5-d3c39ef7a764", "openfda": {"upc": ["0647755015004"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["c422d300-3f4e-4121-8eaf-56683911b884"], "manufacturer_name": ["Zapotol Products Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (59428-604-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59428-604-08", "marketing_start_date": "20201022"}], "brand_name": "All Day Pain Relief", "product_id": "59428-604_9d429a1c-a5e0-4739-80a5-d3c39ef7a764", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59428-604", "generic_name": "Naproxen Sodium", "labeler_name": "Zapotol Products Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20201022", "listing_expiration_date": "20261231"}