HYDROGEN PEROXIDE solution

Hydrogen Peroxide by

Drug Labeling and Warnings

Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Inc, Vi Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrogen peroside (stablized) 3%

Purpose

First aid antiseptic

Use

first aid to help prevent the rist 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 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

SPL UNCLASSIFIED SECTION

Distributed by: CVS Pharmacy, Inc

One CVS Drive, Woonsocket, RI 02895

2011 CVS/pharmacy

www.cvs. com  1-800-shop-CVS

Principal Display Panel

CVS Health

Topical Solution USP

HYDROGEN PEROXIDE

FIRST AID ANTISEPTIC

For treatment of minor cuts + abrasions

8 FL OZ (236 mL)

871.001/871AA

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
hydrogen peroxide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-871
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: 59779-871-34	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1992
2	NDC: 59779-871-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1992
3	NDC: 59779-871-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1992
4	NDC: 59779-871-50	710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1992
5	NDC: 59779-871-99	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/1992

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/15/1992

Labeler - CVS Pharmacy, Inc (062312574)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture(59779-871)