azx wellness hand sanitizer
Generic: alcohol
Labeler: asc marketing ltdDrug Facts
Product Profile
Brand Name
azx wellness hand sanitizer
Generic Name
alcohol
Labeler
asc marketing ltd
Dosage Form
GEL
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
73145-012
Product ID
73145-012_0b6e0202-cdf3-d783-e063-6394a90a3bf2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2021-03-22
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73145012
Hyphenated Format
73145-012
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
azx wellness 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
- 2 mL in 1 PACKET (73145-012-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0b6e0202-cdf3-d783-e063-6394a90a3bf2", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["bf0098ab-6c0d-ecd2-e053-2a95a90a670c"], "manufacturer_name": ["ASC Marketing LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 PACKET (73145-012-01)", "package_ndc": "73145-012-01", "marketing_start_date": "20210322"}], "brand_name": "AZX Wellness Hand Sanitizer", "product_id": "73145-012_0b6e0202-cdf3-d783-e063-6394a90a3bf2", "dosage_form": "GEL", "product_ndc": "73145-012", "generic_name": "ALCOHOL", "labeler_name": "ASC Marketing LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AZX Wellness Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210322", "listing_expiration_date": "20261231"}