NDC 10893-510 Naturasil Molluscum Treatment Kit
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 10893-510?
What are the uses for Naturasil Molluscum Treatment Kit?
Which are Naturasil Molluscum Treatment Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
Which are Naturasil Molluscum Treatment 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:
- CEDAR LEAF OIL (UNII: BJ169U4NLG)
- TEA TREE OIL (UNII: VIF565UC2G)
- CASTOR OIL (UNII: D5340Y2I9G)
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL LAURATE (UNII: Y98611C087)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- SODIUM LAURATE (UNII: K146MR5EXO)
- SODIUM MYRISTATE (UNII: 06BLC4V0IV)
- SODIUM OLEATE (UNII: 399SL044HN)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- SORBITOL (UNII: 506T60A25R)
- ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRISODIUM SULFOSUCCINATE (UNII: 085WB9L09N)
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[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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".