Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment
Sulfur
L'oreal Usa Products Inc
Human Otc Drug
NDC 49967-895Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment also known as Sulfur is a human otc drug labeled by 'L'oreal Usa Products Inc'. National Drug Code (NDC) number for Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment is 49967-895. This drug is available in dosage form of Lotion. The names of the active, medicinal ingredients in Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment drug includes Sulfur - 100 mg/mL . The currest status of Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment drug is Active.
Drug Information:
| Drug NDC: | 49967-895 |
| 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: | Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment |
| 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: | Sulfur |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | L'oreal Usa Products Inc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Lotion |
| 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 - 100 mg/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: | 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: | 01 Nov, 2016 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 15 Jan, 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. |
| Application Number: | part333D |
| 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: | L'Oreal USA Products Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 240725
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| 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 NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 49967-895-01 | 1 TUBE in 1 CARTON (49967-895-01) / 20 mL in 1 TUBE | 01 Nov, 2016 | N/A | No |
| 49967-895-02 | 3 mL in 1 PACKET (49967-895-02) | 01 Nov, 2016 | N/A | No |
| 49967-895-03 | 1.5 mL in 1 PACKET (49967-895-03) | 01 Nov, 2016 | N/A | No |
| 49967-895-04 | 3 mL in 1 TUBE (49967-895-04) | 01 Nov, 2016 | N/A | No |
| 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:
Kiehls since 1851 dermatologist solutions breakout control targeted acne spot treatment sulfur sulfur sulfur water niacinamide glycolic acid stearyl alcohol glycerin phenoxyethanol sodium hydroxide peg-100 stearate phenylethyl resorcinol allantoin ethylhexylglycerin
Indications and Usage:
Use for the treatment of acne
Warnings:
Warnings for external use only
Do Not Use:
Warnings for external use only
When Using:
When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. if irritation occurs, only use one topical acne medication at a time. apply only to areas with acne
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 because excessive drying of the skin 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:
Image description
Further Questions:
Questions or comments? call toll free 1-800-946-4453