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 Universal Distribution Center LLC, Jell Pharmaceuticals Pvt Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Hydrogen Peroxide 3%

Purpose

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.

Ask a doctor before use if you have

deep or puncture wounds, animals bites or serious burns

Stop use and ask a doctor if

• the condition persists or gets worse 
• irritation, pain, or redness persists or worsens 
• swelling, rash, or fever develops

Keep out of reach of children.

Is swallowed, get medical help or contact a Poison Control Center right away

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

Other information

keep tightly closed and at controlled room temperature. Do not shake bottle. Hold srayer tip away from face when opening.

Inactive ingredients

purified water

Package Labeling:

INGREDIENTS AND APPEARANCE

3 HYDROGEN PEROXIDE 
hydrogen peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-805
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-805-01	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/10/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/10/2021

Labeler - Universal Distribution Center LLC (019180459)

Registrant - Jell Pharmaceuticals Pvt Ltd. (726025211)

Establishment
Name	Address	ID/FEI	Business Operations
Jell Pharmaceuticals Pvt Ltd.		726025211	manufacture(52000-805)