MAXIM HYDROGEN PEROXIDE- hydrogen peroxide liquid

maxim Hydrogen Peroxide by

Drug Labeling and Warnings

maxim Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by Ostl, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients 

Hydrogen peroxide (stabilized) 3%

Purpose

First aid antiseptic

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

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 

DOSAGE & ADMINISTRATION

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

Inactive ingredient purified water, Phosphoric acid as a stabilizer

STORAGE AND HANDLING

Other information Keep tightly closed and at controlled room temperature.

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

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

MAXIM HYDROGEN PEROXIDE 
hydrogen peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69950-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHOSPHORIC ACID (UNII: E4GA8884NN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69950-005-02	295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/17/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/17/2016

Labeler - Ostl, Inc. (020117798)