NDC 68479-160 Breakout Clearing Daytime Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-160 - Breakout Clearing Daytime Treatment
Product Packages
NDC Code 68479-160-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-160-01
Package Description: 14 mL in 1 TUBE
NDC Code 68479-160-02
Package Description: 1 TUBE in 1 CARTON / 60 mL in 1 TUBE
Product Details
What is NDC 68479-160?
What are the uses for Breakout Clearing Daytime Treatment?
Which are Breakout Clearing Daytime Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Breakout Clearing Daytime Treatment 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)
- NIACINAMIDE (UNII: 25X51I8RD4)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CUCUMBER (UNII: YY7C30VXJT)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- ROSEMARY (UNII: IJ67X351P9)
- BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- GALACTOARABINAN (UNII: SL4SX1O487)
- POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- XANTHAN GUM (UNII: TTV12P4NEE)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Breakout Clearing Daytime Treatment?
- RxCUI: 200009 - benzoyl peroxide 2.5 % Topical Lotion
- RxCUI: 200009 - benzoyl peroxide 25 MG/ML Topical Lotion
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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".