HYDROGEN PEROXIDE solution

Hydrogen Peroxide by

Drug Labeling and Warnings

Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by Target Corp, Vi Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrogen peroxide (stablized) 3%

Purpose

First Aid Antiseptic

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 the body
• longer than one week

Ask a doctor before use if you have

deep or puncture wounds, animal bites or seerious burns

Keep out of reach of children.

If 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.  Holde sprayer tip away from face when opening.

Inactive ingredients

purified water

SPL UNCLASSIFIED SECTION

Dist. by Target Corp., Mpls., MN 55403

Made in U.S.A. with U.S. and foreign components

Questions? Call 1-800-910-6874

Principal Display Panel

Hydrogen

peroxide

topical solution USP

first aid antiseptic

for treatment of minor cuts and abrasions

up & up

10 FL OZ (295 mL)

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
hydrogen peroxide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-871
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: 11673-871-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1989
2	NDC: 11673-871-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1989
3	NDC: 11673-871-72	295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/1989

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/15/1989

Labeler - Target Corp (006961700)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture(11673-871)