dr lift antibacterial hand sanitizer
Generic: ethyl alcohol
Labeler: spa de soleilDrug Facts
Product Profile
Brand Name
dr lift antibacterial hand sanitizer
Generic Name
ethyl alcohol
Labeler
spa de soleil
Dosage Form
GEL
Routes
Active Ingredients
alcohol 168 mL/240mL
Manufacturer
Identifiers & Regulatory
Product NDC
68062-2250
Product ID
68062-2250_436f3a5d-a6a3-615c-e063-6394a90abd10
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2020-07-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680622250
Hyphenated Format
68062-2250
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
dr lift antibacterial hand sanitizer (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 168 mL/240mL
Packaging
- 240 mL in 1 BOTTLE, PUMP (68062-2250-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "436f3a5d-a6a3-615c-e063-6394a90abd10", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["aba006cd-18db-e42f-e053-2995a90a4607"], "manufacturer_name": ["Spa de Soleil"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE, PUMP (68062-2250-1)", "package_ndc": "68062-2250-1", "marketing_start_date": "20200729"}], "brand_name": "Dr Lift Antibacterial Hand Sanitizer", "product_id": "68062-2250_436f3a5d-a6a3-615c-e063-6394a90abd10", "dosage_form": "GEL", "product_ndc": "68062-2250", "generic_name": "ethyl alcohol", "labeler_name": "Spa de Soleil", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr Lift Antibacterial Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "168 mL/240mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200729", "listing_expiration_date": "20261231"}