NDC 14222-2060 Unblemish Control Broad Spectrum Spf 20
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 14222-2060?
What are the uses for Unblemish Control Broad Spectrum Spf 20?
Which are Unblemish Control Broad Spectrum Spf 20 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Unblemish Control Broad Spectrum Spf 20 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ISODODECANE (UNII: A8289P68Y2)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- AZELAIC ACID (UNII: F2VW3D43YT)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL)
- MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
- NORDIHYDROGUAIARETIC ACID, (+/-)- (UNII: 7PZ73W4ZNR)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- TROPOLONE (UNII: 7L6DL16P1T)
- PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F)
- GLYCERIN (UNII: PDC6A3C0OX)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- SQUALANE (UNII: GW89575KF9)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
* Please review the disclaimer below.
[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".