NDC 33992-3038 Foaming Acne Scrub For A Cleaner, Clearer Complexion
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33992 - Greenbrier International Inc.
- 33992-3038 - Foaming Acne Scrub
Product Packages
NDC Code 33992-3038-1
Package Description: 99 g in 1 BOTTLE
Product Details
What is NDC 33992-3038?
What are the uses for Foaming Acne Scrub For A Cleaner, Clearer Complexion?
Which are Foaming Acne Scrub For A Cleaner, Clearer Complexion 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 Foaming Acne Scrub For A Cleaner, Clearer Complexion 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:
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CUPRIC CATION (UNII: 8CBV67279L)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
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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".