hand sanitizer
Generic: alcohol
Labeler: bath concept cosmetics (dongguan) co., ltdDrug Facts
Product Profile
Brand Name
hand sanitizer
Generic Name
alcohol
Labeler
bath concept cosmetics (dongguan) co., ltd
Dosage Form
GEL
Routes
Active Ingredients
alcohol .62 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
61805-110
Product ID
61805-110_089656e4-6de0-7be7-e063-6394a90a7703
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-04-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61805110
Hyphenated Format
61805-110
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
hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .62 mL/mL
Packaging
- 50 mL in 1 BOTTLE (61805-110-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "089656e4-6de0-7be7-e063-6394a90a7703", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["065e083f-3c13-495d-8619-df45c5fce68b"], "manufacturer_name": ["Bath Concept Cosmetics (Dongguan) Co., Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (61805-110-01)", "package_ndc": "61805-110-01", "marketing_start_date": "20200410"}], "brand_name": "Hand Sanitizer", "product_id": "61805-110_089656e4-6de0-7be7-e063-6394a90a7703", "dosage_form": "GEL", "product_ndc": "61805-110", "generic_name": "ALCOHOL", "labeler_name": "Bath Concept Cosmetics (Dongguan) Co., Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200410", "listing_expiration_date": "20261231"}