NDC 68479-806 Age Bright Spot Fader
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc
- 68479-806 - Age Bright Spot Fader
Product Packages
NDC Code 68479-806-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-806-01
Package Description: 6 mL in 1 TUBE
NDC Code 68479-806-02
Package Description: 1 TUBE in 1 CARTON / 15 mL in 1 TUBE
Product Details
What is NDC 68479-806?
What are the uses for Age Bright Spot Fader?
Which are Age Bright Spot Fader UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Age Bright Spot Fader 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)
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PROPANEDIOL (UNII: 5965N8W85T)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- GLYCERETH-26 (UNII: NNE56F2N14)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- HEXYLRESORCINOL (UNII: R9QTB5E82N)
- CLARY SAGE OIL (UNII: 87L0D4U3M0)
- MALIC ACID (UNII: 817L1N4CKP)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- LEMON OIL (UNII: I9GRO824LL)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- LAVANDIN OIL (UNII: 9RES347CKG)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- CARRAGEENAN SODIUM (UNII: 7CY8BVL34N)
- THYMOL (UNII: 3J50XA376E)
- TERPINEOL (UNII: R53Q4ZWC99)
- PULLULAN (UNII: 8ZQ0AYU1TT)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
- PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SEA SALT (UNII: 87GE52P74G)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Age Bright Spot Fader?
- RxCUI: 346298 - salicylic acid 2 % Topical Gel
- RxCUI: 346298 - salicylic acid 0.02 MG/MG Topical Gel
* 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".