OXY RAPID TREATMENT FACE WASH SENSITIVE SKIN MAXIMUM ACTION- benzoyl peroxide cream 
The Mentholatum Company

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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Drug Facts

Active ingredient

Benzoyl peroxide 5%

Purpose

Acne treatment

Uses

treats and helps prevent acne

Warnings

For external use only

Do not use if you

have very sensitive skin
are sensitive to benzoyl peroxide

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 unnecessary sun exposure and use a sunscreen
avoid contact with the eyes, lips, and mouth
avoid contact with hair and dyed fabrics, which may be bleached by this product
skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using this product less frequently or in a lower concentration.

Stop use and ask a doctor if

irritation becomes severe

If pregnant or breast-feeding

ask a health professional before use.

Keep Out of Reach of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet face
apply to hands then work into a lather and massage gently onto face
rinse thoroughly and pat dry
because excessive drying of the skin may occur, start with 1 use daily, then gradually increase to 2 or 3 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 of both products and ask a doctor.
Sensitivity Test: Apply product sparingly to a small affected area for the first 3 days. If no discomfort occurs, follow directions above.

Other information

THIS PRODUCT MAY BLEACH HAIR OR DYED FABRICS
KEEP TIGHTLY CLOSED
avoid storing at temperatures above 100°F (38°C)

Inactive ingredients

anhydrous citric acid, butylene glycol, capryl/capramidopropyl betaine, cetostearyl alcohol, diazolidinyl urea, disodium laureth sulfosuccinate, hydrolyzed soy protein, methylparaben, PEG-8 dimethicone, portulaca oleracea extract, propylparaben, purified water, sodium C14-16 olefin sulfonate, sodium citrate, sodium hydroxide, sodium lauroyl sarcosinate, xanthan gum

Questions?

1-877-636-2677 MON-FRI 9 AM-5 PM (EST)

Principal Display Panel

Oxy Rapid Treatment Face Wash Sensitive Skin
OXY RAPID TREATMENT FACE WASH SENSITIVE SKIN  MAXIMUM ACTION
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-1308
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SHEA BUTTER (UNII: K49155WL9Y)  
CAPRYL/CAPRAMIDOPROPYL BETAINE (UNII: 231H3ZT9NE)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
SOY PROTEIN (UNII: R44IWB3RN5)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
PURSLANE (UNII: M6S840WXG5)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10742-1308-1148 mL in 1 TUBE; Type 0: Not a Combination Product01/01/201508/31/2018
2NDC:10742-1308-2185 mL in 1 TUBE; Type 0: Not a Combination Product01/01/201508/31/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D01/01/201508/31/2018
Labeler - The Mentholatum Company (002105757)

Revised: 11/2016
 
The Mentholatum Company