Lemaitre Sulfur Acne Treatment

Sulfur


Lemaitre Perfumeria Y Jabones Sas
Human Otc Drug
NDC 73098-001
Lemaitre Sulfur Acne Treatment also known as Sulfur is a human otc drug labeled by 'Lemaitre Perfumeria Y Jabones Sas'. National Drug Code (NDC) number for Lemaitre Sulfur Acne Treatment is 73098-001. This drug is available in dosage form of Soap. The names of the active, medicinal ingredients in Lemaitre Sulfur Acne Treatment drug includes Sulfur - 9 g/100g . The currest status of Lemaitre Sulfur Acne Treatment drug is Active.

Drug Information:

Drug NDC: 73098-001
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: Lemaitre Sulfur Acne Treatment
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base: Lemaitre Sulfur
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix: Acne treatment
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
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: Sulfur
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Lemaitre Perfumeria Y Jabones Sas
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Soap
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:SULFUR - 9 g/100g
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: OTC MONOGRAPH FINAL
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: 13 May, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 14 Jun, 2026
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.
Application Number: M006
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
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:Lemaitre Perfumeria y Jabones SAS
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.
UNII:70FD1KFU70
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
73098-001-011 CELLO PACK in 1 BOX (73098-001-01) / 100 g in 1 CELLO PACK13 May, 2019N/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 acne treatment

Product Elements:

Lemaitre sulfur acne treatment sulfur sulfur sulfur sodium chloride titanium dioxide caramel sodium palmate sodium palm kernelate water glycerin etidronic acid edetate sodium edetic acid butylated hydroxytoluene fd&c yellow no. 5

Indications and Usage:

Uses for the treatment of acne dries and clears acne blemishes, acne pimples, blackheads and whiteheads helps prevent new acne blemishes, acne pimples, blackheads and whiteheads from forming

Warnings:

Warnings for external use only do not use on broken skin large areas of the skin when using this product avoid contact with the eyes apply only to areas with acne skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time. if irritation occurs, use only one topical acne medication at a time. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.

Do Not Use:

Warnings for external use only do not use on broken skin large areas of the skin when using this product avoid contact with the eyes apply only to areas with acne skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time. if irritation occurs, use only one topical acne medication at a time. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.

When Using:

When using this product avoid contact with the eyes apply only to areas with acne skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time. if irritation occurs, use only one topical acne medication at a time.

Dosage and Administration:

Directions clean the skin thoroughly before applying this product cover the entire affected area with a thin layer one to three times daily. rinse thoroughly because excessive dryness may occur, start with one application daily, then gradually increase to two or three times daily if needed, or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Package Label Principal Display Panel:

Lemaitre 100% vegetable oil soap sulfur soap acne treatment deeply cleanses your skin effective action net wt. 3.5 oz (100g) sulfur soap final


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.