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
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Chain Drug Marketing Association

Identifiers & Regulatory

Product NDC 83324-081
Product ID 83324-081_1ac6e721-4d0a-0396-e063-6294a90a7fe9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-04-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324081
Hyphenated Format 83324-081

Supplemental Identifiers

RxCUI
198440
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 PACKAGE in 1 CARTON (83324-081-01) / 100 TABLET in 1 PACKAGE
  • 100 TABLET in 1 BOTTLE, PLASTIC (83324-081-10)
  • 1 BOTTLE, PLASTIC in 1 CARTON (83324-081-60) / 60 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

83324-081-01 1 PACKAGE in 1 CARTON (83324-081-01) / 100 TABLET in 1 PACKAGE 83324-081-10 100 TABLET in 1 BOTTLE, PLASTIC (83324-081-10) 83324-081-60 1 BOTTLE, PLASTIC in 1 CARTON (83324-081-60) / 60 TABLET 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": "1ac6e721-4d0a-0396-e063-6294a90a7fe9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["cfaf9495-e654-4dfc-ba23-d2358c3720c4"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 PACKAGE in 1 CARTON (83324-081-01)  / 100 TABLET in 1 PACKAGE", "package_ndc": "83324-081-01", "marketing_start_date": "20240426"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (83324-081-10)", "package_ndc": "83324-081-10", "marketing_start_date": "20240612"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-081-60)  / 60 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "83324-081-60", "marketing_start_date": "20240426"}], "brand_name": "Pain Relief Extra Strength", "product_id": "83324-081_1ac6e721-4d0a-0396-e063-6294a90a7fe9", "dosage_form": "TABLET", "product_ndc": "83324-081", "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": "20240426", "listing_expiration_date": "20261231"}