instant hand sanitizer
Generic: alcohol
Labeler: ltc products inc.Drug Facts
Product Profile
Brand Name
instant hand sanitizer
Generic Name
alcohol
Labeler
ltc products inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
61598-450
Product ID
61598-450_4833a063-4f8f-9c79-e063-6394a90aa562
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2012-10-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61598450
Hyphenated Format
61598-450
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
- 70 mL/100mL
Packaging
- 118 mL in 1 CYLINDER (61598-450-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4833a063-4f8f-9c79-e063-6394a90aa562", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["6c16aeec-bef2-41f1-b22d-ac37c3625562"], "manufacturer_name": ["LTC Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 CYLINDER (61598-450-04)", "package_ndc": "61598-450-04", "marketing_start_date": "20121012"}], "brand_name": "Instant Hand Sanitizer", "product_id": "61598-450_4833a063-4f8f-9c79-e063-6394a90aa562", "dosage_form": "GEL", "product_ndc": "61598-450", "generic_name": "Alcohol", "labeler_name": "LTC Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Instant Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20121012", "listing_expiration_date": "20271231"}