NDC 64942-1247 St. Ives Green Tea Scrub
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 64942-1247?
What are the uses for St. Ives Green Tea Scrub?
Which are St. Ives Green Tea Scrub 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 St. Ives Green Tea Scrub 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)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
- SODIUM METHYL 2-SULFOLAURATE (UNII: I39GGJ23HV)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERETH-18 ETHYLHEXANOATE (UNII: IWS58C6V2Y)
- DISODIUM 2-SULFOLAURATE (UNII: 329M3829G2)
- KAOLIN (UNII: 24H4NWX5CO)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- GLYCERETH-18 (UNII: SA5E43C17C)
- PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- YEAST (UNII: 3NY3SM6B8U)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for St. Ives Green Tea Scrub?
- RxCUI: 1038982 - salicylic acid 1 % Medicated Liquid Soap
- RxCUI: 1038982 - salicylic acid 10 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".