NDC 11084-061 Debmed Antimicrobial Body Wash And Shampoo
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 11084-061?
What are the uses for Debmed Antimicrobial Body Wash And Shampoo?
Which are Debmed Antimicrobial Body Wash And Shampoo UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Debmed Antimicrobial Body Wash And Shampoo 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)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GUAR GUM (UNII: E89I1637KE)
- ALLANTOIN (UNII: 344S277G0Z)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Debmed Antimicrobial Body Wash And Shampoo?
- RxCUI: 1087960 - triclosan 0.7 % Medicated Liquid Soap
- RxCUI: 1087960 - triclosan 7 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".