NDC 42851-158 Zo Medical Zo Non-hydroquinone Hyperpigmentation System For Skin Brightening
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42851-158?
What are the uses for Zo Medical Zo Non-hydroquinone Hyperpigmentation System For Skin Brightening?
Which are Zo Medical Zo Non-hydroquinone Hyperpigmentation System For Skin Brightening 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 Medical Zo Non-hydroquinone Hyperpigmentation System For Skin Brightening 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)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SODIUM DIHYDROXYCETYL PHOSPHATE (UNII: YWI33EV595)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- MELANIN SYNTHETIC (TYROSINE, PEROXIDE) (UNII: O0CV1RMR44)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ERYTHRITOL (UNII: RA96B954X6)
- HOMARINE HYDROCHLORIDE (UNII: 8866LNG61N)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- NEPHELIUM LAPPACEUM FRUIT RIND (UNII: Y0513T90FO)
- SOYBEAN (UNII: L7HT8F1ZOD)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
* 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".