NDC 83490-901 Lactomedi Self-care Trial Kit
Lactobacillus Ferment Lysate Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 83490-901?
What are the uses for Lactomedi Self-care Trial Kit?
Which are Lactomedi Self-care Trial Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIMOSILACTOBACILLUS FERMENTUM ME-3 (UNII: BQX4W45LG8)
- LIMOSILACTOBACILLUS FERMENTUM ME-3 (UNII: BQX4W45LG8) (Active Moiety)
Which are Lactomedi Self-care Trial 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:
- CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
- WATER (UNII: 059QF0KO0R)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ARTEMISIA VULGARIS WHOLE (UNII: JDR81QW9ZQ)
- MELALEUCA ALTERNIFOLIA WHOLE (UNII: 976KV4FXYF)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
- VINCETOXICUM ATRATUM WHOLE (UNII: U3176B0S5J)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- CHAMOMILE (UNII: FGL3685T2X)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- ACONITIC ACID (UNII: 93371T1BXP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PROPANEDIOL (UNII: 5965N8W85T)
- ADENOSINE (UNII: K72T3FS567)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
* 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.
[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".