NDC 68479-140 Oil Clearing Matte Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-140 - Oil Clearing Matte Moisturizer
Product Packages
NDC Code 68479-140-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-140-01
Package Description: 14 mL in 1 TUBE
NDC Code 68479-140-02
Package Description: 1 TUBE in 1 CARTON / 59 mL in 1 TUBE
Product Details
What is NDC 68479-140?
What are the uses for Oil Clearing Matte Moisturizer?
Which are Oil Clearing Matte Moisturizer 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Oil Clearing Matte Moisturizer 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- ORANGE OIL (UNII: AKN3KSD11B)
- CORIANDER OIL (UNII: 7626GC95E5)
- CITRUS AURANTIIFOLIA SEED OIL (UNII: EW089HAI77)
- BITTER ORANGE OIL (UNII: 9TLV70SV6I)
- CITRUS SINENSIS FLOWER OIL (UNII: AJ56JP5TFP)
- CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
- LEMON OIL (UNII: I9GRO824LL)
- CARDAMOM OIL (UNII: JM0KJ091HZ)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- CLOVE LEAF OIL (UNII: VCA5491KVF)
- LAVANDIN OIL (UNII: 9RES347CKG)
- CLARY SAGE OIL (UNII: 87L0D4U3M0)
- GINGER OIL (UNII: SAS9Z1SVUK)
- ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- BETULA PUBESCENS BARK (UNII: 3R504894L9)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- NYLON-12 (UNII: 446U8J075B)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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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".