sanix alcohol hand rub
Generic: alcohol
Labeler: topiderm, incDrug Facts
Product Profile
Brand Name
sanix alcohol hand rub
Generic Name
alcohol
Labeler
topiderm, inc
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol .62 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51326-900
Product ID
51326-900_2af17da6-253d-4958-92ce-2dc70987b669
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2020-03-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51326900
Hyphenated Format
51326-900
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
sanix alcohol hand rub (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .62 mL/mL
Packaging
- 240 mL in 1 BOTTLE (51326-900-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2af17da6-253d-4958-92ce-2dc70987b669", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["a4fbb714-4f20-400a-ab98-f1c8807ce6fc"], "manufacturer_name": ["Topiderm, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (51326-900-08)", "package_ndc": "51326-900-08", "marketing_start_date": "20200317"}], "brand_name": "Sanix Alcohol Hand Rub", "product_id": "51326-900_2af17da6-253d-4958-92ce-2dc70987b669", "dosage_form": "LIQUID", "product_ndc": "51326-900", "generic_name": "Alcohol", "labeler_name": "Topiderm, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sanix Alcohol Hand Rub", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200317", "listing_expiration_date": "20261231"}