NDC 68479-000 Solar Defense Booster Spf50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-000 - Solar Defense Booster
Product Characteristics
Product Packages
NDC Code 68479-000-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-000-02
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 50 mL in 1 BOTTLE, PLASTIC
NDC Code 68479-000-04
Package Description: 125 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 68479-000?
What are the uses for Solar Defense Booster Spf50?
Which are Solar Defense Booster Spf50 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 Solar Defense Booster Spf50 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- NYLON-12 (UNII: 446U8J075B)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- LEMON PEEL (UNII: 72O054U628)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALLANTOIN (UNII: 344S277G0Z)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SQUALANE (UNII: GW89575KF9)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- HERRING SPERM DNA (UNII: 51FI676N6F)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* 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".