good sense pain relief
Generic: acetaminophen
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
good sense pain relief
Generic Name
acetaminophen
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2574
Product ID
71335-2574_c63f110d-2671-4e48-ba82-b3cd5510268a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
1989-08-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352574
Hyphenated Format
71335-2574
Supplemental Identifiers
RxCUI
UNII
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
good sense pain relief (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (71335-2574-1) / 100 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c63f110d-2671-4e48-ba82-b3cd5510268a", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["c226205d-7c3c-49af-b3e2-fc7b09ad7857"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71335-2574-1) / 100 TABLET in 1 BOTTLE", "package_ndc": "71335-2574-1", "marketing_start_date": "20250205"}], "brand_name": "good sense pain relief", "product_id": "71335-2574_c63f110d-2671-4e48-ba82-b3cd5510268a", "dosage_form": "TABLET", "product_ndc": "71335-2574", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "good sense pain relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19890815", "listing_expiration_date": "20261231"}