rexall pain relief
Generic: acetaminophen
Labeler: dolgencorp, llcDrug Facts
Product Profile
Brand Name
rexall pain relief
Generic Name
acetaminophen
Labeler
dolgencorp, llc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55910-701
Product ID
55910-701_bebe404c-279e-4bbe-9154-35297aa1a275
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2010-08-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910701
Hyphenated Format
55910-701
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
rexall pain relief (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (55910-701-62) / 24 TABLET in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (55910-701-78) / 100 TABLET in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bebe404c-279e-4bbe-9154-35297aa1a275", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["9783cf37-3a2b-4ca1-b4eb-6d6ba047a325"], "manufacturer_name": ["Dolgencorp, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-701-62) / 24 TABLET in 1 BOTTLE", "package_ndc": "55910-701-62", "marketing_start_date": "20100807"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-701-78) / 100 TABLET in 1 BOTTLE", "package_ndc": "55910-701-78", "marketing_start_date": "20100807"}], "brand_name": "rexall pain relief", "product_id": "55910-701_bebe404c-279e-4bbe-9154-35297aa1a275", "dosage_form": "TABLET", "product_ndc": "55910-701", "generic_name": "Acetaminophen", "labeler_name": "Dolgencorp, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "rexall pain relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100807", "listing_expiration_date": "20261231"}