OXY  TOTAL CARE CLARIFYING MOISTURIZER- benzoyl peroxide lotion 
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 2.5%

Purpose

Benzoyl peroxide – Acne treatment

Keep Out of Reach of Children

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

Uses

Warnings

For external use only.

Do not use if you

When using this product

Stop use and ask a doctor if irritation becomes severe.

If pregnant or breast-feeding, ask a health professional before use.

Directions

Other information

Inactive Ingredients

water, glycerin, butylene glycol, carbomer, chlorphenesin, citric acid, dimethyl isosorbide, disodium EDTA, hyaluronic acid, hydrolyzed algin, lauryl methacrylate/glycol dimethacrylate crosspolymer, PEG/PPG-4/12 dimethicone, phenoxyethanol, phytic acid, portulaca oleracea extract, silanetriol, sodium citrate, sodium hydroxide, xanthan gum, zinc sulfate

Questions?1-877-636-2677

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Package/Label Principal Display Panel

Oxy Total Care Clarifying Moisturizer
OXY   TOTAL CARE CLARIFYING MOISTURIZER
benzoyl peroxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-1314
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
HYALURONIC ACID (UNII: S270N0TRQY)  
ALGINIC ACID (UNII: 8C3Z4148WZ)  
LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H)  
PEG/PPG-4/12 DIMETHICONE (UNII: JAN3585W85)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FYTIC ACID (UNII: 7IGF0S7R8I)  
PURSLANE (UNII: M6S840WXG5)  
SILANETRIOL (UNII: E52D0J3TS5)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ZINC SULFATE HEPTAHYDRATE (UNII: N57JI2K7WP)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10742-1314-11 in 1 CARTON09/30/2019
1100 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D09/30/2019
Labeler - The Mentholatum Company (002105757)
Registrant - The Mentholatum Company (002105757)
Establishment
NameAddressID/FEIBusiness Operations
The Mentholatum Company002105757manufacture(10742-1314)

Revised: 2/2023
Document Id: f41fa0d6-27fa-a8d8-e053-2a95a90a1422
Set id: 4568b5d1-efde-4b2f-b7cc-8d227d05dfa1
Version: 3
Effective Time: 20230207
 
The Mentholatum Company