NDC 65753-504 Coretex Professional Outdoor Skin Protection Wallet
Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65753 - Coretex Products Inc
- 65753-504 - Coretex Professional Outdoor Skin Protection Wallet
Product Characteristics
Product Packages
NDC Code 65753-504-36
Package Description: 1 KIT in 1 KIT * 44.4 mL in 1 APPLICATOR * 1.1 mL in 1 POUCH * 1 mL in 1 POUCH * 3.5 mL in 1 POUCH * 7 g in 1 POUCH * 44 mL in 1 PACKET (65753-100-37)
Product Details
What is NDC 65753-504?
What are the uses for Coretex Professional Outdoor Skin Protection Wallet?
Which are Coretex Professional Outdoor Skin Protection Wallet UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- ZINC ACETATE (UNII: FM5526K07A)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Coretex Professional Outdoor Skin Protection Wallet 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:
- PROPYLENE GLYCOL 1-ALLYL ETHER (UNII: QRB8092KPK)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLCELLULOSE (1500 CPS) (UNII: P0NTE48364)
- ALLANTOIN (UNII: 344S277G0Z)
- FRAGARIA VESCA FRUIT (UNII: CG6IX3GCMU)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- CITRULLUS COLOCYNTHIS FRUIT (UNII: 0E49E3V9U6)
- RUBUS IDAEUS SEED (UNII: M3CL7US2ZG)
- HELIANTHUS ANNUUS SEEDCAKE (UNII: 482WYF7XLC)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- MYRCIARIA DUBIA FRUIT (UNII: YSW4EM1EKP)
- VACCINIUM MACROCARPON WHOLE (UNII: D11KO7O2DX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 1,3-PROPANEDIOL BIS(4-AMINOBENZOATE) (UNII: 8860R9ORQR)
- CANNABIS SATIVA SEED (UNII: QE567Z26NG)
- PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)
- EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP)
- HIPPOPHAE RHAMNOIDES FRUIT JUICE (UNII: UC3P08EB3Y)
- PROPYLENE GLYCOL 1-BUTYRATE (UNII: PUV901J64H)
- VACCINIUM ANGUSTIFOLIUM WHOLE (UNII: R3538BZ1BW)
- ACTINIDIA CHINENSIS WHOLE (UNII: 8HTD3WU8LH)
- BRASSICA OLERACEA VAR. ITALICA WHOLE (UNII: DW4954EP53)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PEG-100 STEARATE (UNII: YD01N1999R)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- COMFREY LEAF (UNII: DG4F8T839X)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- EDETIC ACID (UNII: 9G34HU7RV0)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)
- CHAMOMILE (UNII: FGL3685T2X)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TROLAMINE (UNII: 9O3K93S3TK)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- COCONUT OIL (UNII: Q9L0O73W7L)
- WHITE WAX (UNII: 7G1J5DA97F)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCOA BUTTER (UNII: 512OYT1CRR)
What is the NDC to RxNorm Crosswalk for Coretex Professional Outdoor Skin Protection Wallet?
- RxCUI: 1039474 - ethanol 62.5 % Topical Solution
- RxCUI: 1039474 - ethanol 0.625 ML/ML Topical Solution
- RxCUI: 1043353 - benzocaine 6 % Medicated Pad
- RxCUI: 1043353 - benzocaine 60 MG/ML Medicated Pad
- RxCUI: 1043353 - benzocaine 6 % Medicated Wipe
* 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.
[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".