Prevention Wound and Burn
- Manufacturer
- Prevention Health Sciences, Inc.
- Effective date
- 2021-12-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:24:23
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Hydrogen peroxide 3%
Menthol 0.1%
OTC - PURPOSE SECTION
Purpose
First aid antiseptic
Topical analgesic
INDICATIONS & USAGE SECTION
Uses first aid to help prevent infection in minor cuts, scrapes and burns.
WARNINGS SECTION
Warnings
For external use only
OTC - DO NOT USE SECTION
Do not use
- in or near eyes
- over large areas of the body
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
OTC - STOP USE SECTION
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
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
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 SECTION
Inactive ingredients citric acid, deionized water, edetate disodium, glycerin, peppermint oil, saccharin sodium, SD alcohol, sodium citrate,sodium lauryl sulfate, zinc chloride
OTC - QUESTIONS SECTION
Questions? (800) 473-1205
SPL UNCLASSIFIED SECTION
Manufactured by:
Prevention Health Sciences, Inc.
Raleigh, IL 62977
PACKAGE LABEL.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
Products#
Every source-derived product name is available through these pages.
- Prevention Wound and Burn
- Hydrogen peroxide, Menthol
- GLYCERIN
- SACCHARIN SODIUM
- SACCHARIN
- ALCOHOL
- MENTHOL
- SODIUM LAURYL SULFATE
- HYDROGEN PEROXIDE
- CITRIC ACID MONOHYDRATE
- WATER
- EDETATE DISODIUM
- PEPPERMINT OIL
- SODIUM CITRATE
- ZINC CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69951-003 | 69951-003-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| SACCHARIN SODIUM | SB8ZUX40TY | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| SODIUM LAURYL SULFATE | 368GB5141J | IACT |
| HYDROGEN PEROXIDE | BBX060AN9V | ACTIB |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| WATER | 059QF0KO0R | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| PEPPERMINT OIL | AV092KU4JH | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| ZINC CHLORIDE | 86Q357L16B | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d2955050-a0cc-3e0b-e053-2a95a90a07c3 | 8426bd35-372a-4417-e053-2a91aa0a7903 | 2021-12-07 | Warnings | d2955050-a0cc-3e0b-e053-2a95a90a07c3 8426bd35-372a-4417-e053-2a91aa0a7903 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
