NDC 83819-030 Dermveda Complete Lice Treatment Natural Serum

Eucalyptus Globulus Liquid Topical - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
83819-030
Proprietary Name:
Dermveda Complete Lice Treatment Natural Serum
Non-Proprietary Name: [1]
Eucalyptus Globulus
Substance Name: [2]
Eucalyptus Globulus Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Labeler Name: [5]
    Labeler Code:
    83819
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-20-2023
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 83819-030?

    The NDC code 83819-030 is assigned by the FDA to the product Dermveda Complete Lice Treatment Natural Serum which is a human over the counter drug product labeled by Celcius Corp.. The generic name of Dermveda Complete Lice Treatment Natural Serum is eucalyptus globulus. The product's dosage form is liquid and is administered via topical form. The product is distributed in a single package with assigned NDC code 83819-030-04 118 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Dermveda Complete Lice Treatment Natural Serum?

    • Important: Read warnings before use.adults and children 2 years and over • Treat • apply thoroughly to dry hair or other affected area. For head lice, first apply behind ears and to back of neck. • allow product to remain for 60 minutes. • wash area thoroughly with warm water and soap or shampoo • Remove lice and their eggs (nits) • use a fine-tooth or comb. • Remove any remaining nits by hand (using a throw-away glove). • hair should remain slightly damp while removing nits. If hair dries during combing, dampen slightly with water. • Use often within a week to kill newly hatched lice.Children under 2 years ask a Doctor.

    What are Dermveda Complete Lice Treatment Natural Serum Active Ingredients?

    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.

    Which are Dermveda Complete Lice Treatment Natural Serum UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
    • EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)

    Which are Dermveda Complete Lice Treatment Natural Serum 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:

    * Please review the disclaimer below.

    Product Footnotes

    [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".