Hydrogen Peroxide 3% Spray

Hydrogen Peroxide by

Drug Labeling and Warnings

Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by Delon Laboratories (1990) Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HYDROGEN PEROXIDE- hydrogen peroxide solution 
Delon Laboratories (1990) Ltd

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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Hydrogen Peroxide 3% Spray

Active ingredient

Hydrogen peroxide 3%

Pupose

First aid antiseptic

Uses

  • first aid to help prevent the risk of infection in minor cuts, scrapes, and burns

Warnings

For external use only

Do not use

  • in the eyes or apply over large areas of the body
  • longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

  • deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

  • the condition persists or gets worse

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

Directions

  • clean the affected area
  • apply a small amount of this product on the area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other information

  • keep tightly closed in a cool dark place
  • do not shake bottle
  • hold away from face when opening

Inactive ingredient

purified water

Delon Hydrogen Peroxide 3% Spray

Delon Hydrogen Peroxide 3% 3.38 fl oz

HYDROGEN PEROXIDE 
hydrogen peroxide solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 61734-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE3 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 61734-010-08100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/17/202010/20/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/17/202010/20/2022
Labeler - Delon Laboratories (1990) Ltd (248364184)
Establishment
NameAddressID/FEIBusiness Operations
Delon Laboratories (1990) Ltd243387722label(61734-010) , manufacture(61734-010) , pack(61734-010)

Revised: 11/2022
Document Id: ecfcb08f-26e6-19ce-e053-2995a90a7b8e
Set id: b453f52b-3b9d-c0aa-e053-2995a90ad381
Version: 4
Effective Time: 20221108