good sense pain relief
Generic: acetaminophen
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
good sense pain relief
Generic Name
acetaminophen
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-238
Product ID
82804-238_b4cb4a62-9ef7-4185-8770-e9a806c2fb3f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2022-01-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804238
Hyphenated Format
82804-238
Supplemental Identifiers
RxCUI
UPC
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
- 4 POUCH in 1 BAG (82804-238-08) / 2 TABLET in 1 POUCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b4cb4a62-9ef7-4185-8770-e9a806c2fb3f", "openfda": {"upc": ["0382804238088"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["b4cb4a62-9ef7-4185-8770-e9a806c2fb3f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 POUCH in 1 BAG (82804-238-08) / 2 TABLET in 1 POUCH", "package_ndc": "82804-238-08", "marketing_start_date": "20250826"}], "brand_name": "Good Sense Pain Relief", "product_id": "82804-238_b4cb4a62-9ef7-4185-8770-e9a806c2fb3f", "dosage_form": "TABLET", "product_ndc": "82804-238", "generic_name": "Acetaminophen", "labeler_name": "Proficient Rx LP", "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": "20220123", "listing_expiration_date": "20261231"}