NDC 68479-012 Protection 50 Sport
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-012 - Protection 50 Sport
Product Characteristics
Product Packages
NDC Code 68479-012-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-012-01
Package Description: 22 mL in 1 TUBE
NDC Code 68479-012-02
Package Description: 1 TUBE in 1 CARTON / 156 mL in 1 TUBE
Product Details
What is NDC 68479-012?
What are the uses for Protection 50 Sport?
Which are Protection 50 Sport UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Protection 50 Sport 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- CETEARYL PHOSPHATE (UNII: 4O6GCK4CTJ)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".