NDC 68479-005 Concealing Spot Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-005 - Concealing Spot Treatment
Product Characteristics
Product Packages
NDC Code 68479-005-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-005-01
Package Description: 3 mL in 1 TUBE
NDC Code 68479-005-02
Package Description: 1 TUBE in 1 CARTON / 10 mL in 1 TUBE
Product Details
What is NDC 68479-005?
What are the uses for Concealing Spot Treatment?
Which are Concealing Spot Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Concealing Spot 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:
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- ETHYL TRISILOXANE (UNII: ZH1WJO5481)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- NIACINAMIDE (UNII: 25X51I8RD4)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- BIOTIN (UNII: 6SO6U10H04)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- PANTHENOL (UNII: WV9CM0O67Z)
- MONTMORILLONITE (UNII: A585MN1H2L)
- CAFFEINE (UNII: 3G6A5W338E)
- LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- SARCOSINE (UNII: Z711V88R5F)
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- POTASSIUM ALUM (UNII: 1L24V9R23S)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Concealing Spot Treatment?
- RxCUI: 422938 - sulfur 5 % Topical Lotion
- RxCUI: 422938 - sulfur 50 MG/ML Topical Lotion
* Please review the disclaimer below.
[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".