extra strength pain relief

Generic: acetaminophen

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength pain relief
Generic Name acetaminophen
Labeler rite aid corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-5311
Product ID 11822-5311_f8db8ccf-613e-4e6f-8f6f-7207f7e30fcc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2005-12-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118225311
Hyphenated Format 11822-5311

Supplemental Identifiers

RxCUI
198440
UPC
0011822030304
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 extra strength 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 (11822-5311-2) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11822-5311-5) / 50 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (2)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f8db8ccf-613e-4e6f-8f6f-7207f7e30fcc", "openfda": {"upc": ["0011822030304"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["00c121ff-141d-410b-8632-c884a3909552"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-5311-2)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-5311-2", "marketing_start_date": "20051211"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-5311-5)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-5311-5", "marketing_start_date": "20051211"}], "brand_name": "Extra Strength pain relief", "product_id": "11822-5311_f8db8ccf-613e-4e6f-8f6f-7207f7e30fcc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "11822-5311", "generic_name": "Acetaminophen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength pain relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20051211", "listing_expiration_date": "20261231"}