NDC 68715-367 Dermadoctor Dd Eye Spf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68715 - Dermadoctor
- 68715-367 - Dermadoctor Dd Eye
Product Packages
NDC Code 68715-367-02
Package Description: 1 TUBE in 1 CARTON / 15 mL in 1 TUBE (68715-367-01)
Product Details
What is NDC 68715-367?
What are the uses for Dermadoctor Dd Eye Spf30?
Which are Dermadoctor Dd Eye Spf30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Dermadoctor Dd Eye Spf30 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:
- ALBIZIA JULIBRISSIN BARK (UNII: 0J9G6W44DV)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
- ARGANIA SPINOSA SEED (UNII: 8H7X7XB54H)
- LEVOMENOL (UNII: 24WE03BX2T)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAFFEINE (UNII: 3G6A5W338E)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- CERAMIDE NG (UNII: C04977SRJ5)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- COCONUT OIL (UNII: Q9L0O73W7L)
- DARUTOSIDE (UNII: EG8ODI0780)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MICA (UNII: V8A1AW0880)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- PALMITOYL HEXAPEPTIDE-12 (UNII: HO4ZT5S86C)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
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[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".