HYDROGEN PEROXIDE solution

Hydrogen Peroxide by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Hydrogen peroxide (stabilized) 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 body
• longer than one week

Ask a doctor before use if you have

deep or pucture 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
• apply a small amount of the 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

Manufactured for Big Lots By: Vi-Jon, LLC.

8515 Page Avenue St. Louis, MO 63114

V#425040 Item# 100051394

Principal Panel Display

SOUNDBODY

First Aid Antiseptic

HYDROGEN

PEROXIDE

Topical Solution

3% USP

First Aid Antiseptic

32 FL OZ (1 QT) 946mL

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
hydrogen peroxide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50594-871
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: 50594-871-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014
2	NDC: 50594-871-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014
3	NDC: 50594-871-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/08/2014

Labeler - Sound Body (017885351)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(50594-871)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(50594-871)