Label: GET CLARITY FOAMING ACNE CLEANSER- sulfur cream
- NDC Code(s): 69366-413-30
- Packager: The Honest Company, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 19, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
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 • avoid contact with eyes. If contact occurs, rinse thoroughly with water • apply only to areas with acne.
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DOSAGE & ADMINISTRATION
Directions
• Apply a small amount to wet face and work product into a lather. Massage onto face avoiding eye area. Rinse thoroughly with water and pat dry. Use morning and night.
• 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.
- SPL UNCLASSIFIED SECTION
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INACTIVE INGREDIENT
Inactive ingredients
Water (Aqua/Eau), Cocamidopropyl Hydroxysultaine, Bentonite, Sodium Laurylglucosides Hydroxypropylsulfonate, Glycerin, Disodium Cocoyl Glutamate, Sodium Chloride, Sodium Cocoyl Isethionate, Acacia Senegal Gum, Pyrus Malus (Apple) Fruit Extract, Caprylyl Glycol, Glutamic Acid, Malic Acid, Glycolic Acid, Lactic Acid, Coconut Acid, Xanthan Gum, Sodium Cocoyl Glycinate, Caprylhydroxamic Acid, Trisodium Ethylenediamine Disuccinate, Quartz, Citric Acid, Sodium Benzoate.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GET CLARITY FOAMING ACNE CLEANSER
sulfur creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69366-413 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 3.3 g in 100 mL Inactive Ingredients Ingredient Name Strength LACTIC ACID (UNII: 33X04XA5AT) SODIUM COCOYL GLYCINATE (UNII: XLU9KH03XM) SODIUM BENZOATE (UNII: OJ245FE5EU) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) BENTONITE (UNII: A3N5ZCN45C) SODIUM LAURYLGLUCOSIDES HYDROXYPROPYLSULFONATE (UNII: Z6GFR7R72Y) GLYCERIN (UNII: PDC6A3C0OX) DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A) MALIC ACID, L- (UNII: J3TZF807X5) SODIUM CHLORIDE (UNII: 451W47IQ8X) ACACIA (UNII: 5C5403N26O) APPLE (UNII: B423VGH5S9) XANTHAN GUM (UNII: TTV12P4NEE) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) GLUTAMIC ACID (UNII: 3KX376GY7L) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) COCONUT ACID (UNII: 40U37V505D) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCOLIC ACID (UNII: 0WT12SX38S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69366-413-30 1 in 1 CARTON 05/01/2022 1 118.2 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 Drug M006 05/01/2022 Labeler - The Honest Company, Inc (969962757)