NDC 20890-0120 Topcare Antibacterial White Tea Foaming Hand
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 20890-0120?
What are the uses for Topcare Antibacterial White Tea Foaming Hand?
Which are Topcare Antibacterial White Tea Foaming Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Topcare Antibacterial White Tea Foaming Hand 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)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ISOSTEARAMIDOPROPYL ETHYLDIMONIUM ETHOSULFATE (UNII: U059JNZ17L)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE SODIUM (UNII: MP1J8420LU)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- ZINC SULFATE MONOHYDRATE (UNII: PTX099XSF1)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Topcare Antibacterial White Tea Foaming Hand?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
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[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".