Label: ACNE TREATMENT WITH SULFUR- sulfur ointment
- NDC Code(s): 24286-1573-1, 24286-1573-2
- Packager: DLC Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 10, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
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Directions
- cleanse the skin thoroughly before applying
- cover the entire affected area with a thin layer
- leave on for 10 minutes
- thoroughly remove with water
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to 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 ingredient
- Questions
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 74 g Tube Label
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INGREDIENTS AND APPEARANCE
ACNE TREATMENT WITH SULFUR
sulfur ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24286-1573 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 5 g in 100 g Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24286-1573-1 74 g in 1 TUBE; Type 0: Not a Combination Product 08/16/2019 2 NDC:24286-1573-2 6 g in 1 JAR; Type 0: Not a Combination Product 09/13/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/16/2019 Labeler - DLC Laboratories, Inc. (093351930)