pain relief
Generic: acetaminophen
Labeler: meijer, inc.Drug Facts
Product Profile
Brand Name
pain relief
Generic Name
acetaminophen
Labeler
meijer, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
79481-0302
Product ID
79481-0302_09e4aea0-f446-457e-ab21-d0589db5d78f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-06-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
794810302
Hyphenated Format
79481-0302
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
pain relief (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (79481-0302-1) / 100 TABLET, FILM COATED in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09e4aea0-f446-457e-ab21-d0589db5d78f", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["1319bab8-8f17-44fb-9d91-099b0ba38a8d"], "manufacturer_name": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79481-0302-1) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "79481-0302-1", "marketing_start_date": "20240621"}], "brand_name": "PAIN RELIEF", "product_id": "79481-0302_09e4aea0-f446-457e-ab21-d0589db5d78f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "79481-0302", "generic_name": "acetaminophen", "labeler_name": "Meijer, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PAIN RELIEF", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240621", "listing_expiration_date": "20261231"}