NDC 67938-2073 Ceramide Lift And Firm Makeup Broad Spectrum Sunscreen Spf 15 True Beige
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 67938-2073?
What are the uses for Ceramide Lift And Firm Makeup Broad Spectrum Sunscreen Spf 15 True Beige?
Which are Ceramide Lift And Firm Makeup Broad Spectrum Sunscreen Spf 15 True Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Ceramide Lift And Firm Makeup Broad Spectrum Sunscreen Spf 15 True Beige 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:
- ACETYL OCTAPEPTIDE-3 (UNII: 8K14HJF88S)
- ALANINE (UNII: OF5P57N2ZX)
- ALPINIA ZERUMBET LEAF (UNII: MS8P33AMKX)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CERAMIDE 1 (UNII: 5THT33P7X7)
- CERAMIDE 3 (UNII: 4370DF050B)
- CERAMIDE 6 II (UNII: F1X8L2B00J)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ICODEXTRIN (UNII: 2NX48Z0A9G)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FRUCTOSE (UNII: 6YSS42VSEV)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- MANNITOL (UNII: 3OWL53L36A)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MICA (UNII: V8A1AW0880)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- SORBITOL (UNII: 506T60A25R)
- SUCROSE (UNII: C151H8M554)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TREHALOSE (UNII: B8WCK70T7I)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- UREA (UNII: 8W8T17847W)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ZINC STEARATE (UNII: H92E6QA4FV)
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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".