extra strength pain relief
Generic: acetaminophen
Labeler: st. mary's medical park pharmacyDrug Facts
Product Profile
Brand Name
extra strength pain relief
Generic Name
acetaminophen
Labeler
st. mary's medical park pharmacy
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60760-910
Product ID
60760-910_31ce5c80-1530-12a1-e063-6394a90ab119
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
1989-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60760910
Hyphenated Format
60760-910
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
extra strength pain relief (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 50 TABLET in 1 BOTTLE, PLASTIC (60760-910-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31ce5c80-1530-12a1-e063-6394a90ab119", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["31ce5c80-152f-12a1-e063-6394a90ab119"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (60760-910-50)", "package_ndc": "60760-910-50", "marketing_start_date": "20250328"}], "brand_name": "Extra Strength Pain Relief", "product_id": "60760-910_31ce5c80-1530-12a1-e063-6394a90ab119", "dosage_form": "TABLET", "product_ndc": "60760-910", "generic_name": "Acetaminophen", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "19890101", "listing_expiration_date": "20261231"}