NDC 77586-001 Dmi Cosmetics Wash Me Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77586 - Derma Innovation Company Limited
- 77586-001 - Dmi Cosmetics Wash Me Hand Sanitizer
Product Packages
NDC Code 77586-001-01
Package Description: 30 mL in 1 TUBE
NDC Code 77586-001-02
Package Description: 50 mL in 1 TUBE
NDC Code 77586-001-03
Package Description: 400 mL in 1 BOTTLE, PUMP
NDC Code 77586-001-04
Package Description: 450 mL in 1 BOTTLE, PUMP
NDC Code 77586-001-05
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 77586-001?
What are the uses for Dmi Cosmetics Wash Me Hand Sanitizer?
Which are Dmi Cosmetics Wash Me Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Dmi Cosmetics Wash Me Hand Sanitizer 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- IMIDUREA (UNII: M629807ATL)
What is the NDC to RxNorm Crosswalk for Dmi Cosmetics Wash Me Hand Sanitizer?
- 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".