instant hand sanitizer
Generic: alcohol
Labeler: safetec of america, inc.Drug Facts
Product Profile
Brand Name
instant hand sanitizer
Generic Name
alcohol
Labeler
safetec of america, inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol .7 g/mL
Manufacturer
Identifiers & Regulatory
Product NDC
61010-4111
Product ID
61010-4111_129de921-3817-daaf-e063-6394a90a7b9c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2010-12-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
610104111
Hyphenated Format
61010-4111
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
instant hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .7 g/mL
Packaging
- 1026000 mL in 1 CONTAINER (61010-4111-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "129de921-3817-daaf-e063-6394a90a7b9c", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["0f6f2a67-4fed-407e-a2c5-51574a5bbf65"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1026000 mL in 1 CONTAINER (61010-4111-1)", "package_ndc": "61010-4111-1", "marketing_start_date": "20101216"}], "brand_name": "Instant Hand Sanitizer", "product_id": "61010-4111_129de921-3817-daaf-e063-6394a90a7b9c", "dosage_form": "GEL", "product_ndc": "61010-4111", "generic_name": "alcohol", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Instant Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 g/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20101216", "listing_expiration_date": "20261231"}