advanced hand sanitizer
Generic: ethyl alcohol
Labeler: meijer, inc.Drug Facts
Product Profile
Brand Name
advanced hand sanitizer
Generic Name
ethyl alcohol
Labeler
meijer, inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
41250-370
Product ID
41250-370_4b33a939-c22a-ff10-e063-6294a90adca5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
1992-04-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41250370
Hyphenated Format
41250-370
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 hand sanitizer (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 (41250-370-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b33a939-c22a-ff10-e063-6294a90adca5", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["a56b4a66-3923-4e40-a461-1d97043fb89a"], "manufacturer_name": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (41250-370-16)", "package_ndc": "41250-370-16", "marketing_start_date": "19920424"}], "brand_name": "Advanced Hand Sanitizer", "product_id": "41250-370_4b33a939-c22a-ff10-e063-6294a90adca5", "dosage_form": "GEL", "product_ndc": "41250-370", "generic_name": "Ethyl alcohol", "labeler_name": "Meijer, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19920424", "listing_expiration_date": "20271231"}