NDC 78223-006 Wash Free Quick Dry Cleaning Hand Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78223 - Guangzhou Bamianxi Biotechnology Co., Ltd
- 78223-006 - Wash Free Quick Dry Cleaning Hand Gel
Product Packages
NDC Code 78223-006-01
Package Description: 30 mL in 1 BOTTLE
NDC Code 78223-006-02
Package Description: 50 mL in 1 BOTTLE
NDC Code 78223-006-03
Package Description: 60 mL in 1 BOTTLE
NDC Code 78223-006-04
Package Description: 100 mL in 1 BOTTLE
NDC Code 78223-006-05
Package Description: 120 mL in 1 BOTTLE
NDC Code 78223-006-06
Package Description: 200 mL in 1 BOTTLE
NDC Code 78223-006-07
Package Description: 250 mL in 1 BOTTLE
NDC Code 78223-006-08
Package Description: 300 mL in 1 BOTTLE
NDC Code 78223-006-09
Package Description: 500 mL in 1 BOTTLE
NDC Code 78223-006-10
Package Description: 750 mL in 1 BOTTLE
NDC Code 78223-006-11
Package Description: 1000 mL in 1 BOTTLE
NDC Code 78223-006-12
Package Description: 5000 mL in 1 BOTTLE
Product Details
What is NDC 78223-006?
What are the uses for Wash Free Quick Dry Cleaning Hand Gel?
Which are Wash Free Quick Dry Cleaning Hand Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Wash Free Quick Dry Cleaning Hand Gel Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Wash Free Quick Dry Cleaning Hand Gel?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 ML/ML Topical Gel
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".