instant antiseptic hand sanitizer
Generic: alcohol
Labeler: united laboratories inc.Drug Facts
Product Profile
Brand Name
instant antiseptic hand sanitizer
Generic Name
alcohol
Labeler
united laboratories inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
63998-364
Product ID
63998-364_27c4d9c7-c2e6-27c3-e063-6394a90ab384
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2019-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63998364
Hyphenated Format
63998-364
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 antiseptic 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
- 750 mL in 1 BOTTLE (63998-364-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "27c4d9c7-c2e6-27c3-e063-6394a90ab384", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["582753"], "spl_set_id": ["f91a5ac5-0f78-4cf5-be57-6562714791cd"], "manufacturer_name": ["United Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "750 mL in 1 BOTTLE (63998-364-01)", "package_ndc": "63998-364-01", "marketing_start_date": "20190101"}], "brand_name": "Instant Antiseptic Hand Sanitizer", "product_id": "63998-364_27c4d9c7-c2e6-27c3-e063-6394a90ab384", "dosage_form": "SOLUTION", "product_ndc": "63998-364", "generic_name": "Alcohol", "labeler_name": "United Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Instant Antiseptic Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}