NDC 40046-0061 Mineralize Moisture Spf 15 Foundation
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 40046-0061?
What are the uses for Mineralize Moisture Spf 15 Foundation?
Which are Mineralize Moisture Spf 15 Foundation 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 Mineralize Moisture Spf 15 Foundation 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)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- SQUALANE (UNII: GW89575KF9)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LYSINE (UNII: K3Z4F929H6)
- SHEA BUTTER (UNII: K49155WL9Y)
- HABERLEA RHODOPENSIS LEAF (UNII: N042Q65701)
- TAMARIND SEED (UNII: 6AHP8A7OML)
- BETA VULGARIS (UNII: 4G174V5051)
- YEAST (UNII: 3NY3SM6B8U)
- PHYTANTRIOL (UNII: 8LVI07A72W)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- TREHALOSE (UNII: B8WCK70T7I)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- UREA (UNII: 8W8T17847W)
- TRIACETIN (UNII: XHX3C3X673)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".