pain relief extra strength

Generic: acetaminophen

Labeler: discount drug mart
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief extra strength
Generic Name acetaminophen
Labeler discount drug mart
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
DISCOUNT DRUG MART

Identifiers & Regulatory

Product NDC 53943-104
Product ID 53943-104_288cbf57-1697-5f70-e063-6394a90af83b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 53943104
Hyphenated Format 53943-104

Supplemental Identifiers

RxCUI
198440
UPC
0093351118890
UNII
362O9ITL9D

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 pain relief extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (53943-104-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (53943-104-04) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-104-06)
  • 2 BOTTLE, PLASTIC in 1 CARTON (53943-104-09) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (4)

53943-104-02 1 BOTTLE, PLASTIC in 1 CARTON (53943-104-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 53943-104-04 1 BOTTLE, PLASTIC in 1 CARTON (53943-104-04) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 53943-104-06 500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-104-06) 53943-104-09 2 BOTTLE, PLASTIC in 1 CARTON (53943-104-09) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "288cbf57-1697-5f70-e063-6394a90af83b", "openfda": {"upc": ["0093351118890"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["e6fee238-0b6f-cb84-e053-2995a90a361b"], "manufacturer_name": ["DISCOUNT DRUG MART"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (53943-104-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "53943-104-02", "marketing_start_date": "20221001"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (53943-104-04)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "53943-104-04", "marketing_start_date": "20221001"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-104-06)", "package_ndc": "53943-104-06", "marketing_start_date": "20221001"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (53943-104-09)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "53943-104-09", "marketing_start_date": "20221001"}], "brand_name": "Pain Relief Extra Strength", "product_id": "53943-104_288cbf57-1697-5f70-e063-6394a90af83b", "dosage_form": "TABLET, COATED", "product_ndc": "53943-104", "generic_name": "Acetaminophen", "labeler_name": "DISCOUNT DRUG MART", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221001", "listing_expiration_date": "20261231"}