NDC 42851-168 Zo Skin Health Aggressive Anti-aging Program
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42851-168?
What are the uses for Zo Skin Health Aggressive Anti-aging Program?
Which are Zo Skin Health Aggressive Anti-aging Program UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Zo Skin Health Aggressive Anti-aging Program 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:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- WATER (UNII: 059QF0KO0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- BEHENYL BEHENATE (UNII: K8NU647RJ0)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- URIDINE MONOPHOSPHATE DISODIUM (UNII: KD8E20071T)
- ETHYL FERULATE (UNII: 5B8915UELW)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MELANIN SYNTHETIC (TYROSINE, PEROXIDE) (UNII: O0CV1RMR44)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ROSEMARY (UNII: IJ67X351P9)
- SQUALANE (UNII: GW89575KF9)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".