NDC 51389-122 Laura Geller Beauty Sun Kissed Color Lip Balm Trio Broad Spectrum Spf 15 Pink - Coral - Berry
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What is NDC 51389-122?
What are the uses for Laura Geller Beauty Sun Kissed Color Lip Balm Trio Broad Spectrum Spf 15 Pink - Coral - Berry?
Which are Laura Geller Beauty Sun Kissed Color Lip Balm Trio Broad Spectrum Spf 15 Pink - Coral - Berry UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Laura Geller Beauty Sun Kissed Color Lip Balm Trio Broad Spectrum Spf 15 Pink - Coral - Berry 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
- MICA (UNII: V8A1AW0880)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ETHYL VANILLIN (UNII: YC9ST449YJ)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)
- ETHYLHEXYL COCOATE (UNII: I1MPW273QS)
- COCONUT OIL (UNII: Q9L0O73W7L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C RED NO. 6 (UNII: 481744AI4O)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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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".