advanced
Generic: ethyl alcohol
Labeler: perrigo direct, incDrug Facts
Product Profile
Brand Name
advanced
Generic Name
ethyl alcohol
Labeler
perrigo direct, inc
Dosage Form
GEL
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
75981-370
Product ID
75981-370_4b313078-2c80-5e87-e063-6394a90a1972
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2012-09-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75981370
Hyphenated Format
75981-370
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
advanced (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- 59 mL in 1 BOTTLE, PLASTIC (75981-370-16)
- 236 mL in 1 BOTTLE, PLASTIC (75981-370-34)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b313078-2c80-5e87-e063-6394a90a1972", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["68eca241-acce-4f12-9643-bec9b14f53d0"], "manufacturer_name": ["Perrigo Direct, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (75981-370-16)", "package_ndc": "75981-370-16", "marketing_start_date": "20120920"}, {"sample": false, "description": "236 mL in 1 BOTTLE, PLASTIC (75981-370-34)", "package_ndc": "75981-370-34", "marketing_start_date": "20120920"}], "brand_name": "Advanced", "product_id": "75981-370_4b313078-2c80-5e87-e063-6394a90a1972", "dosage_form": "GEL", "product_ndc": "75981-370", "generic_name": "Ethyl Alcohol", "labeler_name": "Perrigo Direct, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120920", "listing_expiration_date": "20271231"}