Lice Ladies Prevent

Sabadilla


Lice Ladies Atlanta, Llc
Human Otc Drug
NDC 70413-555
Lice Ladies Prevent also known as Sabadilla is a human otc drug labeled by 'Lice Ladies Atlanta, Llc'. National Drug Code (NDC) number for Lice Ladies Prevent is 70413-555. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Lice Ladies Prevent drug includes Schoenocaulon Officinale Seed - 6 [hp_X]/mL . The currest status of Lice Ladies Prevent drug is Active.

Drug Information:

Drug NDC: 70413-555
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Lice Ladies Prevent
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Sabadilla
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Lice Ladies Atlanta, Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Spray
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:SCHOENOCAULON OFFICINALE SEED - 6 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 01 Jan, 2011
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 23 Dec, 2025
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.
Listing Expiration Date: 31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Lice Ladies Atlanta, LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0650348991845
UPC stands for Universal Product Code.
UNII:6NAF1689IO
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
70413-555-99237 mL in 1 BOTTLE, SPRAY (70413-555-99)01 Jan, 2011N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Purpose aids in prevention of head lice

Product Elements:

Lice ladies prevent sabadilla schoenocaulon officinale seed schoenocaulon officinale seed water castor oil peppermint oil polysorbate 20 glycerin

Indications and Usage:

Use to aid in the prevention of head lice and nits.

Warnings:

Warnings for external use only. use this product only as directed. if pregnant or nursing, consult with a doctor before use. do not use if live lice are detected. use lice ladies evict™ treatment mousse first! do not use near eyes, nose, inside of mouth, or on eyebrows or eyelashes. consult a doctor if lice is in these areas. when using this product, keep eyes closed tightly and protect eyes with a washcloth or towel. if accidental eye contact occurs, flush eyes thoroughly with water immediately for 5 minutes. stop use and ask a doctor if eye, skin or scalp irritation occurs or continues. keep out of reach of children. in case of ingestion, call poison control center hot-line immediately at 1-800-222-1222. do not use if product has been tampered with.

Dosage and Administration:

Directions: read warnings and directions completely. for adults and children 12 months of age or older. shake well before use. liberally mist onto dry hair from front hairline, behind ears, crown and nape of neck. work down onto the scalp. product will dry naturally. product is safe for daily use and can also be used multiple times in one day.

Package Label Principal Display Panel:

Packaging liceladies-555

Further Questions:

Questions? 1-888-924-5423, 9am-6pm est m-f


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.