NATURIUM SULFUR SPOT TREATMENT 8%- sulfur liquid 
e.l.f. Cosmetics, Inc

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Naturium Sulfur Spot Treatment 8%

Drug Facts

Active Ingredient

Sulfur 8.0%

Purpose

Acne treatment

Uses

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.

Do not use on

  • broken skin
  • large areas of the skin

Keep out of reach of children.


Directions

Shake Well

Other Information

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.Store in controlled temperatures (4-20°C/39-68°F). Keep in a dark and dry place. Keep container tightly closed.

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

1

NATURIUM SULFUR SPOT TREATMENT 8% 
sulfur liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-120
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR80 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76354-120-011 in 1 CARTON06/17/2022
115 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00606/17/2022
Labeler - e.l.f. Cosmetics, Inc (093902816)

Revised: 11/2023
Document Id: 0a276d4e-4adf-2437-e063-6294a90aae21
Set id: 0a4a9aed-5eeb-f648-e063-6394a90a1d76
Version: 1
Effective Time: 20231114
 
e.l.f. Cosmetics, Inc