NDC 64141-009 Rich Lip Color Spf 12
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 64141-009?
Which are Rich Lip Color Spf 12 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Rich Lip Color Spf 12 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:
- OCTYLDODECANOL (UNII: 461N1O614Y)
- DIPENTAERYTHRITYL HEXACAPRYLATE/HEXACAPRATE (UNII: 554N82UWVW)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
- PARAFFIN (UNII: I9O0E3H2ZE)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- IRVINGIA GABONENSIS SEED (UNII: 0J4W1PR213)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- VANILLIN (UNII: CHI530446X)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICA (UNII: V8A1AW0880)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- COCHINEAL (UNII: TZ8Z31B35M)
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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".