NDC 68479-801 Dynamic Skin Recovery Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-801 - Dynamic Skin Recovery
Product Packages
NDC Code 68479-801-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-801-02
Package Description: 1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE
NDC Code 68479-801-04
Package Description: 118 mL in 1 BOTTLE
NDC Code 68479-801-05
Package Description: 10 mL in 1 BOTTLE
NDC Code 68479-801-06
Package Description: 7 mL in 1 BOTTLE
Product Details
What is NDC 68479-801?
What are the uses for Dynamic Skin Recovery Spf 50?
Which are Dynamic Skin Recovery Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Dynamic Skin Recovery Spf 50 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)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- ROSEWOOD OIL (UNII: F2522O5L7B)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- LEMON OIL (UNII: I9GRO824LL)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LEMON PEEL (UNII: 72O054U628)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SQUALANE (UNII: GW89575KF9)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- UREA (UNII: 8W8T17847W)
- GALACTOARABINAN (UNII: SL4SX1O487)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- 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".