zep fuzion instant hand sanitizer
Generic: alcohol
Labeler: zep inc.Drug Facts
Product Profile
Brand Name
zep fuzion instant hand sanitizer
Generic Name
alcohol
Labeler
zep inc.
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
66949-119
Product ID
66949-119_46de5f99-ebe7-c5ae-e063-6394a90a1bbb
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-11-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66949119
Hyphenated Format
66949-119
Supplemental Identifiers
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
zep fuzion 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
- 4800 mL in 1 CASE (66949-119-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "46de5f99-ebe7-c5ae-e063-6394a90a1bbb", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["b43c5701-22ee-1de4-e053-2995a90a8f64"], "manufacturer_name": ["Zep Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4800 mL in 1 CASE (66949-119-16)", "package_ndc": "66949-119-16", "marketing_start_date": "20201102"}], "brand_name": "Zep Fuzion Instant Hand Sanitizer", "product_id": "66949-119_46de5f99-ebe7-c5ae-e063-6394a90a1bbb", "dosage_form": "LIQUID", "product_ndc": "66949-119", "generic_name": "Alcohol", "labeler_name": "Zep Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zep Fuzion Instant Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201102", "listing_expiration_date": "20261231"}