pain relief
Generic: acetaminophen
Labeler: discount drug martDrug Facts
Product Profile
Brand Name
pain relief
Generic Name
acetaminophen
Labeler
discount drug mart
Dosage Form
TABLET, COATED
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
53943-304
Product ID
53943-304_288998e3-a490-9c47-e063-6394a90ae9aa
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2010-01-05
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53943304
Hyphenated Format
53943-304
Supplemental Identifiers
RxCUI
UPC
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
- 500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-304-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "288998e3-a490-9c47-e063-6394a90ae9aa", "openfda": {"upc": ["0093351118890"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["972f09a7-2aa1-4b1b-a6dc-2c4578a07803"], "manufacturer_name": ["DISCOUNT DRUG MART"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-304-06)", "package_ndc": "53943-304-06", "marketing_start_date": "20100105"}], "brand_name": "Pain Relief", "product_id": "53943-304_288998e3-a490-9c47-e063-6394a90ae9aa", "dosage_form": "TABLET, COATED", "product_ndc": "53943-304", "generic_name": "Acetaminophen", "labeler_name": "DISCOUNT DRUG MART", "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": "20100105", "listing_expiration_date": "20261231"}