NDC 68759-003 Youth Full Tinted Moisturizer Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68759 - American Beauty Cosmetics
- 68759-003 - Youth Full Tinted Moisturizer
Product Packages
NDC Code 68759-003-01
Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE (68759-003-02)
Product Details
What is NDC 68759-003?
Which are Youth Full Tinted Moisturizer Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Youth Full Tinted Moisturizer Spf 15 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)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- JOJOBA OIL (UNII: 724GKU717M)
- PETROLATUM (UNII: 4T6H12BN9U)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- STEARETH-21 (UNII: 53J3F32P58)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- XANTHAN GUM (UNII: TTV12P4NEE)
- STEARETH-2 (UNII: V56DFE46J5)
- POTASSIUM STEARATE (UNII: 17V812XK50)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBIC ACID (UNII: X045WJ989B)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".