Label: CLARIFYING SPOT WITH SULFUR PLUS GREEN CLAY ACNE MEDICATION- sulfur solution
- NDC Code(s): 72704-129-01
- Packager: Lancer Skincare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 19, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
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
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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.
- Inactive Ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 9 mL Tube Carton
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INGREDIENTS AND APPEARANCE
CLARIFYING SPOT WITH SULFUR PLUS GREEN CLAY ACNE MEDICATION
sulfur solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72704-129 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sulfur (UNII: 70FD1KFU70) (Sulfur - UNII:70FD1KFU70) Sulfur 10 g in 100 mL Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) Water (UNII: 059QF0KO0R) Azelaic Acid (UNII: F2VW3D43YT) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) Green Tea Leaf (UNII: W2ZU1RY8B0) Salicylic Acid (UNII: O414PZ4LPZ) Papain (UNII: A236A06Y32) Bromelains (UNII: U182GP2CF3) Maltodextrin (UNII: 7CVR7L4A2D) Glycerin (UNII: PDC6A3C0OX) Magnesium Aluminum Silicate (UNII: 6M3P64V0NC) Disodium Carboxyethyl Siliconate (UNII: 4U4C79679G) Ledikite (UNII: D7BC5B0F46) Montmorillonite (UNII: A585MN1H2L) Kaolin (UNII: 24H4NWX5CO) Calcium Carbonate (UNII: H0G9379FGK) Sodium Hydroxide (UNII: 55X04QC32I) Chromic Oxide (UNII: X5Z09SU859) Titanium Dioxide (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72704-129-01 1 in 1 CARTON 10/15/2021 1 9 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333D 10/15/2021 Labeler - Lancer Skincare LLC. (079089155) Establishment Name Address ID/FEI Business Operations Vege-Labs 117878620 MANUFACTURE(72704-129)