NDC 70472-102 Triseptin Water Aided
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70472 - Dfb Technology Ltd
- 70472-102 - Triseptin
Product Characteristics
Product Packages
NDC Code 70472-102-32
Package Description: 946 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 70472-102?
What are the uses for Triseptin Water Aided?
Which are Triseptin Water Aided UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Triseptin Water Aided 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:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCAMINE OXIDE (UNII: QWA2IZI6FI)
- GLYCERYL LAURATE (UNII: Y98611C087)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
What is the NDC to RxNorm Crosswalk for Triseptin Water Aided?
- RxCUI: 1809903 - ethanol 70 % Topical Lotion
- RxCUI: 1809903 - ethanol 0.7 ML/ML Topical Lotion
* 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".