NDC 64942-1245 St. Ives Blemish And Blackhead Control Apricot Scrub
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What is NDC 64942-1245?
What are the uses for St. Ives Blemish And Blackhead Control Apricot Scrub?
Which are St. Ives Blemish And Blackhead Control Apricot 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 Blemish And Blackhead Control Apricot 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)
- JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CORN GRAIN (UNII: C1Z9U7094Z)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- TROLAMINE (UNII: 9O3K93S3TK)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PEG-100 STEARATE (UNII: YD01N1999R)
- APRICOT (UNII: 269CJD5GZ9)
- CETYL ACETATE (UNII: 4Q43814HXS)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
- PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
What is the NDC to RxNorm Crosswalk for St. Ives Blemish And Blackhead Control Apricot Scrub?
- RxCUI: 1039716 - St. Ives 2 % Medicated Liquid Soap
- RxCUI: 1039716 - salicylic acid 20 MG/ML Medicated Liquid Soap [St. Ives Blemish & Blackhead Control]
- RxCUI: 1039716 - St. Ives Blemish & Blackhead Control 2 % Medicated Liquid Soap
- RxCUI: 1039716 - St. Ives Blemish & Blackhead Control 20 MG/ML Medicated Liquid Soap
- RxCUI: 1039716 - St. Ives Green Tea 2 % 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".