pain relief extra strength

Generic: acetaminophen

Labeler: dolgencorp, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

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

acetaminophen 500 mg/1

Manufacturer
DOLGENCORP, LLC

Identifiers & Regulatory

Product NDC 55910-812
Product ID 55910-812_ff0f7223-4a62-4f38-99d0-d108f13a8e9a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2004-05-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55910812
Hyphenated Format 55910-812

Supplemental Identifiers

RxCUI
198440
UPC
0350844519320
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
  • 120 TABLET, COATED in 1 BOTTLE, PLASTIC (55910-812-32)
source: ndc

Packages (1)

55910-812-32 120 TABLET, COATED in 1 BOTTLE, PLASTIC (55910-812-32)

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": "ff0f7223-4a62-4f38-99d0-d108f13a8e9a", "openfda": {"upc": ["0350844519320"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ce9f4e0d-43fb-499a-b8a2-a997a14841c4"], "manufacturer_name": ["DOLGENCORP, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE, PLASTIC (55910-812-32)", "package_ndc": "55910-812-32", "marketing_start_date": "20040510"}], "brand_name": "Pain Relief Extra Strength", "product_id": "55910-812_ff0f7223-4a62-4f38-99d0-d108f13a8e9a", "dosage_form": "TABLET, COATED", "product_ndc": "55910-812", "generic_name": "Acetaminophen", "labeler_name": "DOLGENCORP, LLC", "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": "20040510", "listing_expiration_date": "20261231"}