pain relief extra strength

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name pain relief extra strength
Generic Name acetaminophen
Labeler chain drug marketing association
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Chain Drug Marketing Association

Identifiers & Regulatory

Product NDC 63868-084
Product ID 63868-084_243531d9-3c42-d20a-e063-6294a90a2b09
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2014-06-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868084
Hyphenated Format 63868-084

Supplemental Identifiers

RxCUI
198440
UPC
0635515908420
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
  • 500 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-084-05)
  • 1 BOTTLE, PLASTIC in 1 CARTON (63868-084-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (63868-084-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (63868-084-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (4)

63868-084-05 500 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-084-05) 63868-084-10 1 BOTTLE, PLASTIC in 1 CARTON (63868-084-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 63868-084-24 1 BOTTLE, PLASTIC in 1 CARTON (63868-084-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 63868-084-50 1 BOTTLE, PLASTIC in 1 CARTON (63868-084-50) / 50 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": "243531d9-3c42-d20a-e063-6294a90a2b09", "openfda": {"upc": ["0635515908420"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["68a52858-35c5-402a-8ceb-8d8a7c1e5f6c"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-084-05)", "package_ndc": "63868-084-05", "marketing_start_date": "20140613"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-084-10)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-084-10", "marketing_end_date": "20260831", "marketing_start_date": "20140613"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-084-24)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-084-24", "marketing_end_date": "20260831", "marketing_start_date": "20140613"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-084-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-084-50", "marketing_end_date": "20260831", "marketing_start_date": "20140613"}], "brand_name": "Pain Relief Extra Strength", "product_id": "63868-084_243531d9-3c42-d20a-e063-6294a90a2b09", "dosage_form": "TABLET, COATED", "product_ndc": "63868-084", "generic_name": "Acetaminophen", "labeler_name": "Chain Drug Marketing Association", "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": "20140613", "listing_expiration_date": "20261231"}