pain relief

Generic: acetaminophen

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief
Generic Name acetaminophen
Labeler h e b
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-980
Product ID 37808-980_47074aaf-86d0-4a94-afc0-123353ba293b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1991-06-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808980
Hyphenated Format 37808-980

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 (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 in 1 CARTON (37808-980-62) / 24 TABLET in 1 BOTTLE
source: ndc

Packages (1)

37808-980-62 1 BOTTLE in 1 CARTON (37808-980-62) / 24 TABLET in 1 BOTTLE

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": "47074aaf-86d0-4a94-afc0-123353ba293b", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["add6952e-9dd5-487c-93e6-337e9d6a4872"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-980-62)  / 24 TABLET in 1 BOTTLE", "package_ndc": "37808-980-62", "marketing_start_date": "19910615"}], "brand_name": "Pain Relief", "product_id": "37808-980_47074aaf-86d0-4a94-afc0-123353ba293b", "dosage_form": "TABLET", "product_ndc": "37808-980", "generic_name": "Acetaminophen", "labeler_name": "H E B", "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_start_date": "19910615", "listing_expiration_date": "20261231"}