NDC 67938-091 Intervene Makeup Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 67938-091?
What are the uses for Intervene Makeup Spf 15?
Which are Intervene Makeup Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Intervene 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)
- ISODODECANE (UNII: A8289P68Y2)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TALC (UNII: 7SEV7J4R1U)
- SORBITAN TRISTEARATE (UNII: 6LUM696811)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICA (UNII: V8A1AW0880)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- LAURETH-7 (UNII: Z95S6G8201)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- NARCISSUS TAZETTA BULB (UNII: K17762966S)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- LAURETH-4 (UNII: 6HQ855798J)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- STEARETH-20 (UNII: L0Q8IK9E08)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
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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".