advanced hand sanitizer
Generic: ethyl alcohol
Labeler: amerisource bergenDrug Facts
Product Profile
Brand Name
advanced hand sanitizer
Generic Name
ethyl alcohol
Labeler
amerisource bergen
Dosage Form
GEL
Routes
Active Ingredients
alcohol 700 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24385-034
Product ID
24385-034_498dbb02-ae5d-fa3b-e063-6394a90af4ce
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2014-10-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24385034
Hyphenated Format
24385-034
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, PUMP (24385-034-34)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "498dbb02-ae5d-fa3b-e063-6394a90af4ce", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["e2718f0e-14e9-4698-8400-f5dfe9169bf7"], "manufacturer_name": ["Amerisource Bergen"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 BOTTLE, PUMP (24385-034-34)", "package_ndc": "24385-034-34", "marketing_start_date": "20141028"}], "brand_name": "Advanced Hand Sanitizer", "product_id": "24385-034_498dbb02-ae5d-fa3b-e063-6394a90af4ce", "dosage_form": "GEL", "product_ndc": "24385-034", "generic_name": "Ethyl Alcohol", "labeler_name": "Amerisource Bergen", "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": "20141028", "listing_expiration_date": "20271231"}