NDC 68479-800 Daily Defense Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-800 - Daily Defense
Product Characteristics
Product Packages
NDC Code 68479-800-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-800-02
Package Description: 1 TUBE in 1 CARTON / 100 mL in 1 TUBE
Product Details
What is NDC 68479-800?
What are the uses for Daily Defense Spf 15?
Which are Daily Defense Spf 15 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Daily Defense Spf 15 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- N-LACTOYL ETHANOLAMINE (UNII: 900T44YNC7)
- APPLE (UNII: B423VGH5S9)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- MAHONIA AQUIFOLIUM ROOT (UNII: 746TB9VNDP)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- WHEAT GERM (UNII: YR3G369F5A)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PANTHENOL (UNII: WV9CM0O67Z)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- LAVANDIN OIL (UNII: 9RES347CKG)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALLANTOIN (UNII: 344S277G0Z)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- SODIUM NA-22 (UNII: N2511Z637B)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- POLIDRONIUM CHLORIDE (UNII: 6716Z5YR3G)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".