NDC 14743-536 Tahitian Noni Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14743 - Tahitian Noni International
- 14743-536 - Tahitian Noni
Product Packages
NDC Code 14743-536-02
Package Description: 1 BOTTLE in 1 BOX / 200 mL in 1 BOTTLE (14743-536-01)
Product Details
What is NDC 14743-536?
What are the uses for Tahitian Noni Sunscreen Spf 30?
Which are Tahitian Noni Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Tahitian Noni Sunscreen 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:
- MORINDA CITRIFOLIA FRUIT (UNII: 7829X3G2X5)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MORINDA CITRIFOLIA SEED OIL (UNII: 84J6H9QZUA)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GARDENIA TAITENSIS FLOWER (UNII: T0OCU8201Y)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
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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".