HYDROGEN PEROXIDE- 1169 hydrogen peroxide spray spray

Hydrogen Peroxide by

Drug Labeling and Warnings

Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrogen Peroxide USP 3%

Purpose

First Aid Antiseptic

Uses

First aid to help decrease the risk of skin infection in minor cuts, scrapes, and burns

Warnings

For External Use Only

Do not use

In the eyes Over larege areas of the body More than 1 week unless directed by a doctor

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 (1-800-222-1222) right away.

Directions

Clean the affected area Apply a small amount of the product to the affected area 1 to 3 times daily May be covered with a sterile bandage If bandaged, let dry first

Children under 12 years of age: Consult a doctor before use

Other information

Store at 20º-25ºC (68º-77ºF)

Inactive ingredient

Purified Water

Questions?

1-888-Dynarex Monday - Friday, 9AM - 5PM EST.

Label

1169 Label

Label

1364

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
1169 hydrogen peroxide spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	0.03 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-015-07	24 in 1 CASE	02/29/2024
1	NDC: 67777-015-08	59.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 67777-015-05	1000 in 1 CASE	02/29/2024
2	NDC: 67777-015-06	29.6 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	02/29/2024

Labeler - Dynarex Corporation (008124539)