NDC 70415-401 Puro Antibacterial Wash Foam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70415 - Cwgc La Inc.
- 70415-401 - Puro Antibacterial Wash Foam
Product Packages
NDC Code 70415-401-01
Package Description: 1000 mL in 1 BOTTLE
Product Details
What is NDC 70415-401?
What are the uses for Puro Antibacterial Wash Foam?
Which are Puro Antibacterial Wash Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Puro Antibacterial Wash Foam 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Puro Antibacterial Wash Foam?
- RxCUI: 436367 - chloroxylenol 0.5 % Medicated Liquid Soap
- RxCUI: 436367 - chloroxylenol 5 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".