Label: NEUTROGENA STUBBORN ACNE SPOT DRYING- sulfur lotion
- NDC Code(s): 69968-0761-1
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
Flammable: Keep away from fire or flame
When using this product
- Avoid contact with eyes. If contact occurs, immediately flush with water.
- 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.
- Sensitivity Test for a New user: Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.
- Other Information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 29mL Bottle
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INGREDIENTS AND APPEARANCE
NEUTROGENA STUBBORN ACNE SPOT DRYING
sulfur lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0761 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength ZINC OXIDE (UNII: SOI2LOH54Z) STARCH, CORN (UNII: O8232NY3SJ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) NIACINAMIDE (UNII: 25X51I8RD4) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) SALICYLIC ACID (UNII: O414PZ4LPZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0761-1 1 in 1 CARTON 08/01/2022 1 29 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/01/2022 Labeler - Kenvue Brands LLC (118772437)