3% HYDROGEN PEROXIDE- hydrogen peroxide liquid

3% HYDROGEN PEROXIDE by

Drug Labeling and Warnings

3% HYDROGEN PEROXIDE by is a Otc medication manufactured, distributed, or labeled by LJ Pharma. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Hydrogen Peroxide (Stabilized) 3%

Purpose

FIRST AID ANTISEPTIC ORAL DEBRIDING AGENT

Uses

First aid to help prevent the risk of infection in minor cuts, Scrapes & Burns. Aids in the removal of phlegm , mucus or other secretions associated with occasional sore mouth

Warnings

• For external use only
• IF taken internally, Serious gastric disturbances will result.  Flammable , Keep away from fire or flame.
• Use only in a well-ventilated area:Fumes may be toxic.

Ask a doctor before use if you havedeep or puncture wounds, Animal bites or serious burns.

When using this product:

• Do not Apply over large areas of the body.
• Do not use longer than one week unless directed by doctor

Stop use and ask doctor ifconditions persist or get worse

Keep out of reach of children In case of ingestion , get medical help or contact a poison. control center right away.

KEEP OUT OF REACH OF CHILDREN

Directions

• Clean the affected Area
• Apply Small amount of this product on the area 1-3 times daily
• Let the alcohol dry on skin before using bandages.
• May be covered with a sterile bandag.

Other information

• Store ate room temperature
• Do not shake bottle Hold away from face when opening.
• Does not contain, nor is intended as a substitute for grain or ethyl alchol.

Inactive Ingredients

Purified Water

Product label

INGREDIENTS AND APPEARANCE

3% HYDROGEN PEROXIDE 
hydrogen peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84809-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	3 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84809-005-01	12 in 1 CARTON	06/30/2025
1		236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 84809-005-02	12 in 1 CARTON	06/30/2025
2		473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
3	NDC: 84809-005-03	12 in 1 CARTON	08/04/2025
3		946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/30/2025

Labeler - LJ Pharma (914078633)

Establishment
Name	Address	ID/FEI	Business Operations
LJ Pharma		914078633	manufacture(84809-005)