YOUR LOGO HERE ANTISEPTIC SPRAY

Manufacturer
Dixon Investments, Inc.
Effective date
2026-10-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-10-06 02:02:42

Label at a glance#

ProductYour Logo Here Antiseptic First Aid
Active ingredientBENZOCAINE, BENZETHONIUM CHLORIDE
Label structure11 sections

Indications and uses

treatment of minor cuts, scratches and burns pain relief helps prevent infection soothes itching 

Dosage and administration

clean the affected area shake can well before using hold 4-6 inches from surface and spray area until wet for adult institutional use only not intended for use on children 

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 10% w/w
Benzethonium Chloride 0.2% w/w 

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic
Topical Antiseptic 

Uses

INDICATIONS & USAGE SECTION

treatment of minor cuts, scratches and burns
pain relief
helps prevent infection
soothes itching 

Warnings

WARNINGS SECTION

For External Use Only

Flammable

keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

in or near eyes or other mucous membranes
in case of serious burns
in deep puncture wounds
for a prolonged period of time
on large portions of the body 

When using this product

OTHER SAFETY INFORMATION

avoid spraying in the eyes
contents under pressure
do not puncture or incinerate container
do not store at temperatures above 120°F
use only as directed
intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal 

Stop use and ask doctor if

OTC - STOP USE SECTION

redness, swelling, or irritation occurs
infection occurs
condition worsens or symptoms persist for more than 7 days 

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

clean the affected area
shake can well before using
hold 4-6 inches from surface and spray area until wet
for adult institutional use only
not intended for use on children 

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Dipropylene glycol, isobutane, n-butane, and propane

Principal Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZETHONIUM CHLORIDEACTIVE INGREDIENTPH41D057441
BENZOCAINEACTIVE INGREDIENTU3RSY48JW51
BENZETHONIUMACTIVE MOIETY1VU15B70BP1
BENZOCAINEACTIVE MOIETYU3RSY48JW51
BUTANEINACTIVE INGREDIENT6LV4FOR43R1
DIPROPYLENE GLYCOLINACTIVE INGREDIENTE107L85C401
ISOBUTANEINACTIVE INGREDIENTBXR49TP6111
PROPANEINACTIVE INGREDIENTT75W9911L61

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52982-10052982-100-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-01-28full-release2026-06-01 00:53:50

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 14 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
6 equally ranked IID candidates
BUTANEBUTANE6LV4FOR43RAEROSOL / TOPICALNAExact identifier — unii+route
4 equally ranked IID candidates
ISOBUTANEISOBUTANEBXR49TP611AEROSOL, SPRAY / TOPICAL4484 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPANEPROPANET75W9911L6AEROSOL, FOAM / TOPICAL55 %w/wExact identifier — unii+route
2 equally ranked IID candidates
BUTANEBUTANE6LV4FOR43RAEROSOL / TOPICALNAExact identifier — unii+route
4 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
6 equally ranked IID candidates
BUTANEBUTANE6LV4FOR43RAEROSOL, FOAM / TOPICAL27 %w/wExact identifier — unii+route
4 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
6 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
6 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
6 equally ranked IID candidates
BUTANEBUTANE6LV4FOR43RAEROSOL, FOAM / TOPICAL27 %w/wExact identifier — unii+route
4 equally ranked IID candidates
PROPANEPROPANET75W9911L6AEROSOL, FOAM / TOPICAL55 %w/wExact identifier — unii+route
2 equally ranked IID candidates
ISOBUTANEISOBUTANEBXR49TP611AEROSOL, SPRAY / TOPICAL4484 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
6 equally ranked IID candidates

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Your Logo Here Antiseptic First AidBENZOCAINE AND BENZETHONIUM CHLORIDEDixon Investments, Inc.12b32b5e-cef0-47fe-a526-a4a3454fbf682025-01-28WarningsExact identifier
ndc (package): 52982-100-03
ndc (product): 52982-100
ndc11 (package): 52982010003
spl set id: 12b32b5e-cef0-47fe-a526-a4a3454fbf68

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.