NDC 57677-059 Mineral Tinted Moisture Broad Spectrum Spf 15 Oil Free
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57677 - Aveda Coporation
- 57677-059 - Mineral Tinted Moisture
Product Packages
NDC Code 57677-059-01
Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE
Product Details
What is NDC 57677-059?
What are the uses for Mineral Tinted Moisture Broad Spectrum Spf 15 Oil Free?
Which are Mineral Tinted Moisture Broad Spectrum Spf 15 Oil Free 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 Mineral Tinted Moisture Broad Spectrum Spf 15 Oil Free 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)
- TRICAPRYLYL CITRATE (UNII: BXW1GAI4TA)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MICA (UNII: V8A1AW0880)
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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".