NDC 82384-0034 Everyday Superstars Spf Discovery Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 82384-0034 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
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Product Details
What is NDC 82384-0034?
What are the uses for Everyday Superstars Spf Discovery Kit?
Which are Everyday Superstars Spf Discovery Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Everyday Superstars Spf Discovery 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:
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- SHEA BUTTER (UNII: K49155WL9Y)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK)
- ZINC SULFATE, UNSPECIFIED FORM (UNII: 89DS0H96TB)
- DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MANNITOL (UNII: 3OWL53L36A)
- DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF)
- POLYESTER-7 (UNII: 0841698D2F)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ISODODECANE (UNII: A8289P68Y2)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TRIOCTYLDODECYL CITRATE (UNII: 35X8CT063R)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- GLYCERIN (UNII: PDC6A3C0OX)
- SQUALANE (UNII: GW89575KF9)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- LESPEDEZA CAPITATA FLOWERING TOP (UNII: F930LFZ4LF)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- WATER (UNII: 059QF0KO0R)
- PROPANEDIOL (UNII: 5965N8W85T)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- LEMON OIL, COLD PRESSED (UNII: I9GRO824LL)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- ROSEWOOD OIL (UNII: F2522O5L7B)
- ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)
- POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- ALLANTOIN (UNII: 344S277G0Z)
- ROSEMARY (UNII: IJ67X351P9)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BEHENIC ACID (UNII: H390488X0A)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- RICE BRAN (UNII: R60QEP13IC)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- CETYL BEHENATE (UNII: WFM51TRO3E)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- PANTHENOL (UNII: WV9CM0O67Z)
- SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ)
* Please review the disclaimer below.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".