all day relief

Generic: naproxen sodium

Labeler: publix super markets inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day relief
Generic Name naproxen sodium
Labeler publix super markets inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Publix Super Markets Inc

Identifiers & Regulatory

Product NDC 56062-368
Product ID 56062-368_425a8909-6426-4f87-a95d-4ef8e56eb47a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 1997-12-29

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 56062368
Hyphenated Format 56062-368

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 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 (56062-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (56062-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (56062-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

56062-368-62 1 BOTTLE in 1 CARTON (56062-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE 56062-368-71 1 BOTTLE in 1 CARTON (56062-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE 56062-368-75 1 BOTTLE in 1 CARTON (56062-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

All Day Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "425a8909-6426-4f87-a95d-4ef8e56eb47a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["688451a2-e94a-434a-8e9c-9fe3abf5c3d5"], "manufacturer_name": ["Publix Super Markets Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-368-62)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-368-62", "marketing_start_date": "20040212"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-368-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-368-71", "marketing_start_date": "20010315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-368-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-368-75", "marketing_start_date": "20211208"}], "brand_name": "All Day Relief", "product_id": "56062-368_425a8909-6426-4f87-a95d-4ef8e56eb47a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "56062-368", "generic_name": "Naproxen Sodium", "labeler_name": "Publix Super Markets Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "19971229", "listing_expiration_date": "20261231"}