NDC 68479-909 Invisible Physical Defense Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-909 - Invisible Physical Defense Spf 30
Product Packages
NDC Code 68479-909-00
Package Description: 177 mL in 1 TUBE
NDC Code 68479-909-01
Package Description: 1 TUBE in 1 CARTON / 7 mL in 1 TUBE
NDC Code 68479-909-02
Package Description: 50 mL in 1 TUBE
NDC Code 68479-909-04
Package Description: 177 mL in 1 TUBE
Product Details
What is NDC 68479-909?
What are the uses for Invisible Physical Defense Spf 30?
Which are Invisible Physical Defense Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Invisible Physical Defense Spf 30 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- ARGAN OIL (UNII: 4V59G5UW9X)
- OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU)
- TRAMETES VERSICOLOR FRUITING BODY (UNII: 4C900477MT)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- PROPANEDIOL (UNII: 5965N8W85T)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- LEVOMENOL (UNII: 24WE03BX2T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LAVANDIN OIL (UNII: 9RES347CKG)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
* 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".