ACNE VANISHING GEL-10%- benzoyl peroxide gel 
Only Yourx Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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10 % Benzoyl peroxide

To help with the control of acne

WARNING: For external use only

Water, Glycerin, Propylene Glycol, Ethoxydiglycol, Cetyl Octanoate, Glyceryl, Stearate, PEG-100 Stearate, Cetearyl Alcohol, Ceteareth-20, Dimthicone, Polysorbate 20, Laureth-7, Acrylates C10-30 Alkyl Acrylate Crosspolymer, Polyacrylamide C3-14 Isoparaffin, Potassium Sorbate, Triethanolamine, Disodium EDTA, Ethylhexylglycerin, Phenooxyethanol

Treats acne and helps prevent new acne blemishes from forming

Kills acne bacteria

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center

Store at room temperature

Keep tightly closed

Consult a doctor if excessive irritation occurs

Do not use if

When using this product

Acne Vanishing Gel 10%

ACNE VANISHING GEL-10% 
benzoyl peroxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70367-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE10 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL 1-(2-METHYLBUTYRATE) (UNII: 9Q5W5G6461)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
LAURETH-7 (UNII: Z95S6G8201)  
PEG-100 STEARATE (UNII: YD01N1999R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70367-001-0130 mL in 1 TUBE; Type 0: Not a Combination Product08/26/2014
2NDC:70367-001-04120 mL in 1 TUBE; Type 0: Not a Combination Product08/26/2014
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/26/2014
Labeler - Only Yourx Inc. (089207519)

Revised: 1/2020
Document Id: 9cd580b9-bb6a-951a-e053-2995a90a78cd
Set id: 67cc60ff-bacb-0b07-e053-2991aa0a65fe
Version: 2
Effective Time: 20200123
 
Only Yourx Inc.