PREVENTION WOUND AND BURN- hydrogen peroxide, menthol liquid

Prevention Wound and Burn by

Drug Labeling and Warnings

Prevention Wound and Burn by is a Otc medication manufactured, distributed, or labeled by Prevention Health Sciences, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Hydrogen peroxide 3%

Menthol 0.1%

PURPOSE

Purpose

First aid antiseptic

Topical analgesic

INDICATIONS & USAGE

Uses first aid to help prevent infection in minor cuts, scrapes and burns.

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use

• in or near eyes
• over large areas of the body

ASK DOCTOR

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

STOP USE

Stop use and ask a doctor if

• condition gets worse
• symptoms last more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

Adults and children 2 years of age and older:

• clean the affected area
• apply to affected area 1 to 3 times daily
• may be covered with a sterile bandage
• if bandaged, let dry first

Children under 2 years old: ask a doctor

INACTIVE INGREDIENT

Inactive ingredients citric acid, deionized water, edetate disodium, glycerin, peppermint oil, saccharin sodium, SD alcohol, sodium citrate,sodium lauryl sulfate, zinc chloride

QUESTIONS

Questions? (800) 473-1205

SPL UNCLASSIFIED SECTION

Manufactured by:

Prevention Health Sciences, Inc.

Raleigh, IL 62977

PRINCIPAL DISPLAY PANEL

PREVENTION™ WOUND AND BURN

FIRST AID ANTISEPTIC

with Pain Relief

For Minor Cuts, Scrapes & Burns

USED BY PROFESSIONALS

4 FL OZ - 118 ML

INGREDIENTS AND APPEARANCE

PREVENTION WOUND AND BURN 
hydrogen peroxide, menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69951-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	3 g  in 100 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PEPPERMINT OIL (UNII: AV092KU4JH)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC CHLORIDE (UNII: 86Q357L16B)
GLYCERIN (UNII: PDC6A3C0OX)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
ALCOHOL (UNII: 3K9958V90M)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69951-003-04	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/29/2019

Labeler - Prevention Health Sciences, Inc. (968930540)

Establishment
Name	Address	ID/FEI	Business Operations
Prevention Health Sciences, Inc.		968930540	manufacture(69951-003)