advanced hand sanitizer
Generic: ethyl alcohol
Labeler: winco foodsDrug Facts
Product Profile
Brand Name
advanced hand sanitizer
Generic Name
ethyl alcohol
Labeler
winco foods
Dosage Form
GEL
Routes
Active Ingredients
alcohol 700 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
67091-439
Product ID
67091-439_4aa26786-9ed7-646b-e063-6394a90afea6
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2017-07-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67091439
Hyphenated Format
67091-439
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 hand sanitizer (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 700 mg/mL
Packaging
- 236 mL in 1 BOTTLE, DISPENSING (67091-439-34)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4aa26786-9ed7-646b-e063-6394a90afea6", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["25204aac-e940-45dc-804b-81fd141449d7"], "manufacturer_name": ["Winco Foods"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 BOTTLE, DISPENSING (67091-439-34)", "package_ndc": "67091-439-34", "marketing_start_date": "20170703"}], "brand_name": "Advanced Hand Sanitizer", "product_id": "67091-439_4aa26786-9ed7-646b-e063-6394a90afea6", "dosage_form": "GEL", "product_ndc": "67091-439", "generic_name": "Ethyl Alcohol", "labeler_name": "Winco Foods", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "700 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170703", "listing_expiration_date": "20271231"}