MAXIM HYDROGEN PEROXIDE- hydrogen peroxide liquid 
Ostl, 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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maxim SOLUTION OF Hydrogen Peroxide

Drug Facts

Active ingredients 

Hydrogen peroxide (stabilized) 3%

Purpose

First aid antiseptic

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

Use 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 one week

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 

Directions • Clean the affected area • spray a small amount of product on the affected area 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Inactive ingredient purified water, Phosphoric acid as a stabilizer

Other information Keep tightly closed and at controlled room temperature.

Do not shake bottle, Hold sprayer tip away from face when opening.

Hydrogen Peroxide 3% Topical Solution USP

TOPICAL ANTI-INFECTIVE

For treatment of minor cuts and abrasions.

Made in India

Imported by : OSTL Inc.

5805 White Oak Ave Encino CA, 91416

WWW.OSTLTRADE.COM

Packaging

image description

MAXIM HYDROGEN PEROXIDE 
hydrogen peroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69950-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69950-005-02295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/17/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/17/2016
Labeler - Ostl, Inc. (020117798)

Revised: 5/2016
Document Id: cf365a61-6e9c-4ee5-af82-41eb0e218f3c
Set id: d3f63dca-3de0-4805-b8a5-407ec9311b31
Version: 1
Effective Time: 20160522
 
Ostl, Inc.