NDC 82739-007 Hermon Molluscum Contagiosum Treatment Oil
Tea Tree Oil Body Wash Oil Cutaneous - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82739-007?
What are the uses for Hermon Molluscum Contagiosum Treatment Oil?
What are Hermon Molluscum Contagiosum Treatment Oil Active Ingredients?
Which are Hermon Molluscum Contagiosum Treatment Oil UNII Codes?
The UNII codes for the active ingredients in this product are:
- THUJA OCCIDENTALIS BARK (UNII: 19RAD88E6O)
- THUJA OCCIDENTALIS BARK (UNII: 19RAD88E6O) (Active Moiety)
- TEA TREE OIL (UNII: VIF565UC2G)
- TEA TREE OIL (UNII: VIF565UC2G) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- SILVER CATION (UNII: 57N7B0K90A)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- COCO MONOETHANOLAMIDE (UNII: C80684146D) (Active Moiety)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) (Active Moiety)
Which are Hermon Molluscum Contagiosum Treatment Oil 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:
- ALCOHOL (UNII: 3K9958V90M)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- GLYCERIN (UNII: PDC6A3C0OX)
- TEA TREE OIL (UNII: VIF565UC2G)
- WATER (UNII: 059QF0KO0R)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- PAEONIA SUFFRUTICOSA ROOT BARK (UNII: BUG255FE7X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LAURYL SULFATE (UNII: DIQ16UC154)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- PURSLANE (UNII: M6S840WXG5)
- CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0)
- OPUNTIA STREPTACANTHA STEM (UNII: 3TF9Z1U73O)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- POTASSIUM COCOYL GLYCINATE (UNII: WZ70FUF22U)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PANTHENOL (UNII: WV9CM0O67Z)
- TOCOPHEROL (UNII: R0ZB2556P8)
- LEVOMENOL (UNII: 24WE03BX2T)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
* 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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".