HYDROGEN PEROXIDE solution

Hydrogen Peroxide by

Drug Labeling and Warnings

Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by Amerifoods Trading Co, 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 serious burns

Stop use and ask a doctor if

the condition persists or gets worse

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.  Hold sprayer tip away from face when opening.

Inactive ingredients

purified water

adverse reactions

Quality Guaranteed or Your Money Back

DISTRIBUTED BY: AMERIFOODS TRADING CO.

P.O. BOX 512377, LOS ANGELES, CA 90051-0377

871.001/871AA

principal display panel

Iris

Hydrogen

Peroxide

TOPICAL SOLUTION USP

First Aid Antiseptic

For Treatment of

Minor Cuts & Abrasions

NET 128 FL OZ (1 GAL) 3.79 L

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
hydrogen peroxide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61504-871
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: 61504-871-08	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/09/2017
2	NDC: 61504-871-72	295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/09/2017
3	NDC: 61504-871-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/09/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/09/2017

Labeler - Amerifoods Trading Co (626388680)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture(61504-871)