NDC 49520-104 Take Control Calming Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49520-104?
What are the uses for Take Control Calming Cleanser?
Which are Take Control Calming Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Take Control Calming Cleanser 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)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
- GINGER (UNII: C5529G5JPQ)
- OAT (UNII: Z6J799EAJK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CURDLAN (UNII: 6930DL209R)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MENTHOL (UNII: L7T10EIP3A)
- MYRISTOYL PENTAPEPTIDE-4 (UNII: PMA59A699X)
- ACETYL CARBOXYMETHYL COCOYL GLYCINE (UNII: 3TNX4P92J3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
What is the NDC to RxNorm Crosswalk for Take Control Calming Cleanser?
- RxCUI: 562600 - salicylic acid 2 % Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 20 MG/ML Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 2 % Facial Cleanser Toner
- RxCUI: 562600 - salicylic acid 2 % Facial Scrub
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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".