NDC 75936-610 Mineral Spf Starter Kit
Titanium Dioxide,Zinc Oxide Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 75936-610?
What are the uses for Mineral Spf Starter Kit?
Which are Mineral Spf Starter Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Mineral Spf Starter Kit 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)
- SQUALANE (UNII: GW89575KF9)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
- LESPEDEZA CAPITATA FLOWERING TOP (UNII: F930LFZ4LF)
- PROPANEDIOL (UNII: 5965N8W85T)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- POLYGLYCERYL-3 LAURATE (UNII: Y9ZSR39D0E)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ISODODECANE (UNII: A8289P68Y2)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- TRIOCTYLDODECYL CITRATE (UNII: 35X8CT063R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- C9-11 ALKANE/CYCLOALKANE (UNII: 3EZ541F5MW)
- ARUNDINARIA GIGANTEA WHOLE (UNII: 0W60URK9Q6)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- TOCOPHEROL (UNII: R0ZB2556P8)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- HEDYCHIUM CORONARIUM ROOT (UNII: 92A6N0IQN9)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- COCO GLUCOSIDE (UNII: ICS790225B)
- ERYTHRITOL (UNII: RA96B954X6)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- LEVOMENOL (UNII: 24WE03BX2T)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- POLYESTER-7 (UNII: 0841698D2F)
- POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62)
- ETHYL FERULATE (UNII: 5B8915UELW)
- HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- C13-15 ALKANE (UNII: 114P5I43UJ)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- LAURYL LAURATE (UNII: GPW77G0937)
- ASTROCARYUM VULGARE KERNEL OIL (UNII: 1IQY04O559)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".