pain relief

Generic: acetaminophen

Labeler: chain drug consortium
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief
Generic Name acetaminophen
Labeler chain drug consortium
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
CHAIN DRUG CONSORTIUM

Identifiers & Regulatory

Product NDC 68016-502
Product ID 68016-502_2433e9ee-18c9-5a26-e063-6394a90af361
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2008-01-01
Marketing End 2026-06-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68016502
Hyphenated Format 68016-502

Supplemental Identifiers

RxCUI
198440
UPC
0840986021640
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 (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 (68016-502-00) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-502-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

68016-502-00 1 BOTTLE, PLASTIC in 1 CARTON (68016-502-00) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 68016-502-50 1 BOTTLE, PLASTIC in 1 CARTON (68016-502-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2433e9ee-18c9-5a26-e063-6394a90af361", "openfda": {"upc": ["0840986021640"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["cfde9163-ac40-4943-8a9b-509fa5770a93"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-502-00)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-502-00", "marketing_end_date": "20260630", "marketing_start_date": "20080101"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-502-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-502-50", "marketing_end_date": "20260531", "marketing_start_date": "20080101"}], "brand_name": "Pain Relief", "product_id": "68016-502_2433e9ee-18c9-5a26-e063-6394a90af361", "dosage_form": "TABLET, COATED", "product_ndc": "68016-502", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG CONSORTIUM", "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_end_date": "20260630", "marketing_start_date": "20080101"}