NDC 82904-304 I Dew Care Tea Tree O Starterkit
Salicylic Acid Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 82904-304?
What are the uses for I Dew Care Tea Tree O Starterkit?
Which are I Dew Care Tea Tree O Starterkit UNII Codes?
The UNII codes for the active ingredients in this product are:
- TEA TREE OIL (UNII: VIF565UC2G)
- TEA TREE OIL (UNII: VIF565UC2G) (Active Moiety)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are I Dew Care Tea Tree O Starterkit 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:
- OLIVE OIL (UNII: 6UYK2W1W1E)
- APPLE SEED OIL (UNII: 9ACA4K9013)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- BETAINE (UNII: 3SCV180C9W)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- TREHALOSE (UNII: B8WCK70T7I)
- POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)
- ARGININE (UNII: 94ZLA3W45F)
- GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER (300000 CP AT 2%) (UNII: MEA9KH24QG)
- PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CHAMOMILE (UNII: FGL3685T2X)
- COPOVIDONE K25-31 (UNII: D9C330MD8B)
- COCOA (UNII: D9108TZ9KG)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- MONARDA DIDYMA LEAF (UNII: JY15982UBB)
- APPLE (UNII: B423VGH5S9)
- WINE GRAPE (UNII: 3GOV20705G)
- PAPAYA (UNII: KU94FIY6JB)
- PRUNUS MUME FRUIT (UNII: 639190I8CU)
- TEA TREE OIL (UNII: VIF565UC2G)
- 4-TERPINEOL, (+/-)- (UNII: L65MV77ZG6)
- LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
- FRAGRANCE 13576 (UNII: 5EM498GW35)
- ICODEXTRIN (UNII: 2NX48Z0A9G)
- MENTHA SUAVEOLENS LEAF (UNII: 1341ZC68MK)
- MATRICARIA RECUTITA LEAF (UNII: 6I9LN466F0)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- LAMINARIA JAPONICA (UNII: WE98HW412B)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- TROMETHAMINE (UNII: 023C2WHX2V)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- COCO-BETAINE (UNII: 03DH2IZ3FY)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BETA VULGARIS ROOT FRUCTOOLIGOSACCHARIDES (UNII: N2UDM48ZD6)
- LAURYL HYDROXYSULTAINE (UNII: 176KKP31OZ)
- PROPANEDIOL (UNII: 5965N8W85T)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ECLIPTA PROSTRATA LEAF (UNII: H86R96580E)
- TANGERINE PEEL (UNII: JU3D414057)
What is the NDC to RxNorm Crosswalk for I Dew Care Tea Tree O Starterkit?
- RxCUI: 1234456 - salicylic acid 1.5 % Medicated Liquid Soap
- RxCUI: 1234456 - salicylic acid 15 MG/ML Medicated Liquid Soap
* 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".