hand sanitizer
Generic: alcohol
Labeler: veritiv operating companyDrug Facts
Product Profile
Brand Name
hand sanitizer
Generic Name
alcohol
Labeler
veritiv operating company
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
71897-465
Product ID
71897-465_4af55997-9ad8-7443-e063-6294a90a6c35
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2025-08-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71897465
Hyphenated Format
71897-465
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
- 70 mL/100mL
Packaging
- 1000 mL in 1 BOTTLE, PLASTIC (71897-465-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4af55997-9ad8-7443-e063-6294a90a6c35", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["616805"], "spl_set_id": ["3b8a41b3-54c5-f5c0-e063-6394a90a9fac"], "manufacturer_name": ["Veritiv Operating Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (71897-465-86)", "package_ndc": "71897-465-86", "marketing_start_date": "20250804"}], "brand_name": "Hand Sanitizer", "product_id": "71897-465_4af55997-9ad8-7443-e063-6294a90a6c35", "dosage_form": "LIQUID", "product_ndc": "71897-465", "generic_name": "Alcohol", "labeler_name": "Veritiv Operating Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250804", "listing_expiration_date": "20271231"}