HYDROGEN PEROXIDE solution

Hydrogen Peroxide by

Drug Labeling and Warnings

Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by CDMA, Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrogen peroxide (stabilized) 3%

Purpose

First aid antiseptic

Uses

• first aid to help prevent the rise 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, 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 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 ingredient

purified water

Adverse reaction

Distributed by CDMA

Novi, MI 48375

www.qualitychoice.com

Questions: 800-935-2362

principal display panel

NDC: 83324-176-10

QC ®

QUALITY CHOICE

Topical Solution USP

Hydrogen Peroxide

First Aid Antiseptic

For Treatment of Minor Cuts and Abrasions

10 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
hydrogen peroxide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-176
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: 83324-176-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/02/2024
2	NDC: 83324-176-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/02/2024
3	NDC: 83324-176-10	295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	07/02/2024

Labeler - CDMA (011920774)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83324-176)