OXY CLEANSING PADS  DAILY DEFENSE- salicylic acid swab 
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

Salicylic acid 2%

Purpose

Salicylic acid - Acne treatment

Uses

treats and helps prevent acne

Warnings

For external use only

When using this product

  • keep away from eyes, lips and mouth. If contact occurs, flush thoroughly with water.
  • 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.
  • do not leave pad on skin

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

Other information

Inactive ingredients

alcohol (46% v/v), fragrance, isoceteth-20, PEG-8/SMDI copolymer, purified water, trisodium EDTA, trolamine

Questions?

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

Package/Label Principal Display Panel

Oxy Cleansing Pads

Principal Display Panel

Drug Facts
OXY CLEANSING PADS   DAILY DEFENSE
salicylic acid swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-3204
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ISOCETETH-20 (UNII: O020065R7Z)  
PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)  
WATER (UNII: 059QF0KO0R)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10742-3204-190 in 1 JAR; Type 0: Not a Combination Product08/01/2016
2NDC:10742-3204-255 in 1 JAR; Type 0: Not a Combination Product08/01/2016
3NDC:10742-3204-3115 in 1 JAR; Type 0: Not a Combination Product08/01/2016
4NDC:10742-3204-470 in 1 JAR; Type 0: Not a Combination Product08/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/01/2016
Labeler - The Mentholatum Company (002105757)
Registrant - The Mentholatum Company (002105757)
Establishment
NameAddressID/FEIBusiness Operations
The Mentholatum Company002105757manufacture(10742-3204)

Revised: 2/2023
Document Id: f4200b39-1703-4048-e053-2995a90a01e0
Set id: 3e7583e5-7510-4ed9-b454-45924a3526b1
Version: 5
Effective Time: 20230207
 
The Mentholatum Company