Sound Body 871.001/871AA 3% Hydrogen Peroxide

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]

HYDROGEN PEROXIDE- hydrogen peroxide solution 
Sound Body

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Sound Body 871.001/871AA
3% Hydrogen Peroxide

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 1 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 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

Pat. D675, 101

Principal Panel Display

SOUNDBODYâ„¢

First Aid Antiseptic

HYDROGEN PEROXIDE

Topical Solution

3% USP

First Aid Antiseptic

32 FL OZ (1 QT) 946 mL

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)	Â

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	11/03/2019
2	NDC: 50594-871-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014	09/01/2025
3	NDC: 50594-871-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2014	09/24/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/08/2014	09/24/2025

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)

Revised: 9/2025

Document Id: 400a101f-45d2-aeab-e063-6294a90a88de

34390-5

Set id: 88abe157-7ea1-4299-bbcd-b9116c1a25e6

Version: 20

Effective Time: 20250930

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