good sense pain relief
Generic: acetaminophen
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
good sense pain relief
Generic Name
acetaminophen
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7252
Product ID
50090-7252_d758253a-3160-4bd3-929e-7ae9827fcff9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
1989-09-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907252
Hyphenated Format
50090-7252
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
- 500 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (50090-7252-1) / 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": "d758253a-3160-4bd3-929e-7ae9827fcff9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["d9bebb47-6ff4-4ddc-b48f-18f942373484"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-7252-1) / 100 TABLET in 1 BOTTLE", "package_ndc": "50090-7252-1", "marketing_start_date": "20240924"}], "brand_name": "Good Sense Pain Relief", "product_id": "50090-7252_d758253a-3160-4bd3-929e-7ae9827fcff9", "dosage_form": "TABLET", "product_ndc": "50090-7252", "generic_name": "Acetaminophen", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Good Sense Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19890915", "listing_expiration_date": "20261231"}