NDC 49527-010 Continuous Coverage Makeup Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49527-010?
What are the uses for Continuous Coverage Makeup Spf 15?
Which are Continuous Coverage Makeup Spf 15 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 Continuous Coverage Makeup 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)
- TALC (UNII: 7SEV7J4R1U)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- TROMETHAMINE (UNII: 023C2WHX2V)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- POLYAMINOPROPYL BIGUANIDE (UNII: 322U039GMF)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- IRON (UNII: E1UOL152H7)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
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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".