NDC 35192-005 Astringent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 35192 - Ca-botana International
- 35192-005 - Astringent
Product Packages
NDC Code 35192-005-04
Package Description: 4 mL in 1 POUCH
Product Details
What is NDC 35192-005?
What are the uses for Astringent?
Which are Astringent UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM ACETATE (UNII: 80EHD8I43D)
- ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)
Which are Astringent 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCINE (UNII: TE7660XO1C)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- MALIC ACID (UNII: 817L1N4CKP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- STRONTIUM CHLORIDE HEXAHYDRATE (UNII: O09USB7Z44)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Astringent?
- RxCUI: 1594642 - aluminum acetate 0.2 % Topical Gel
- RxCUI: 1594642 - aluminum acetate 0.002 MG/MG 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".