NDC 98132-190 Pure Transformation Sheer Clear
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 98132-190?
What are the uses for Pure Transformation Sheer Clear?
Which are Pure Transformation Sheer Clear 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 Pure Transformation Sheer Clear 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:
- BORON NITRIDE (UNII: 2U4T60A6YD)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- TRIMYRISTIN (UNII: 18L31PSR28)
- BETAINE (UNII: 3SCV180C9W)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALOE (UNII: V5VD430YW9)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALUMINUM DIMYRISTATE (UNII: J2KA067N9O)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CYCLOPIA INTERMEDIA LEAF (UNII: 29UXG2GG8O)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ECTOINE (UNII: 7GXZ3858RY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WHEAT GERM (UNII: YR3G369F5A)
- DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
- FERULIC ACID (UNII: AVM951ZWST)
- LITCHI FRUIT (UNII: Y5P61KP51E)
- RICE GERM (UNII: 7N2B70SFEZ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ROSEMARY (UNII: IJ67X351P9)
- TETRAHYDROBISDEMETHOXYDIFERULOYLMETHANE (UNII: 973IBV8W7I)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
- MICA (UNII: V8A1AW0880)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".