Label: NATURIUM SULFUR SPOT TREATMENT 8%- sulfur liquid
- NDC Code(s): 76354-120-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- 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
- Avoid eye area. In case of eye contact, flush gently and thoroughly with water.
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Directions
Shake Well
- 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.
- if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use and ask a doctor.
- Other Information
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Inactive Ingredients
Aqua (Water), Kaolin, Aluminum Starch Octenylsuccinate, Propanediol, Glyceryl Stearate, Niacinamide, Acacia Senegal Gum, Cetearyl Alcohol, Glycerin, Ganoderma Lucidum Extract, Acetyl Glucosamine, Aloe Barbadensis Leaf Juice, Tranexamic Acid, Citric Acid, Xanthan Gum, Phenoxyethanol, Tocopheryl Acetate, Ethylhexylglycerin, 1,2-Hexanediol, Caprylyl Glycol, Potassium Sorbate, Sodium Benzoate, Tocopherol.
- Product Packaging
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INGREDIENTS AND APPEARANCE
NATURIUM SULFUR SPOT TREATMENT 8%
sulfur liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 80 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) KAOLIN (UNII: 24H4NWX5CO) ALOE VERA LEAF (UNII: ZY81Z83H0X) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PROPANEDIOL (UNII: 5965N8W85T) NIACINAMIDE (UNII: 25X51I8RD4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) TOCOPHEROL (UNII: R0ZB2556P8) ACACIA (UNII: 5C5403N26O) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCERIN (UNII: PDC6A3C0OX) GANODERMA LUCIDUM WHOLE (UNII: J5P04QW0CF) N-ACETYLGLUCOSAMINE (UNII: V956696549) TRANEXAMIC ACID (UNII: 6T84R30KC1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-120-01 1 in 1 CARTON 06/17/2022 1 15 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 06/17/2022 Labeler - e.l.f. Cosmetics, Inc (093902816)