pain relief extra strength

Generic: acetaminophen

Labeler: heb
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

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

acetaminophen 500 mg/1

Manufacturer
HEB

Identifiers & Regulatory

Product NDC 37808-792
Product ID 37808-792_24fec5b0-65f6-5e20-e063-6394a90a66bc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2013-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808792
Hyphenated Format 37808-792

Supplemental Identifiers

RxCUI
198440
UPC
0041220278589
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 (37808-792-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (37808-792-03) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

37808-792-01 1 BOTTLE, PLASTIC in 1 CARTON (37808-792-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 37808-792-03 1 BOTTLE, PLASTIC in 1 CARTON (37808-792-03) / 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": "24fec5b0-65f6-5e20-e063-6394a90a66bc", "openfda": {"upc": ["0041220278589"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["0863aeaa-15ec-4c67-ba79-4dad54555bd2"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-792-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-792-01", "marketing_start_date": "20130201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-792-03)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-792-03", "marketing_start_date": "20130201"}], "brand_name": "Pain Relief Extra Strength", "product_id": "37808-792_24fec5b0-65f6-5e20-e063-6394a90a66bc", "dosage_form": "TABLET, COATED", "product_ndc": "37808-792", "generic_name": "Acetaminophen", "labeler_name": "HEB", "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": "20130201", "listing_expiration_date": "20261231"}