BENZOCAINE,ISOPROPYL ALCOHOL

Manufacturer: Adventure Ready Brands
Effective date: 2021-12-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 22:19:39

Label at a glance#

ProductBENZOCAINE,ISOPROPYL ALCOHOL

Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL

Label structure7 sections

Dosage and administration

Apply to affected area 3-4 times daily. For adults and children 2 years of age and older. Children under 2 years; consult physician.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine, 6% w/v

Isopropyl Alcohol 60% w/v

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Antiseptic

Use

INDICATIONS & USAGE SECTION

For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

in the eyes If contact occurs, flush eyes with water.

Flammable,

SPL UNCLASSIFIED SECTION

keep away from fire or flame.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop

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

Apply to affected area 3-4 times daily. For adults and children 2 years of age and older. Children under 2 years; consult physician.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front Label

Back Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44224-3623-0	2024-12-27	C162847	48780-1	f386c64a-493e-0266-e053-dadaa90a7c1a	After Bite Sting Relief Pad
44224-3623-0	2023-01-30	C162847	48780-1	f386c64a-493e-0266-e053-dadaa90a7c1a	After Bite Sting Relief Pad

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

BENZOCAINE,ISOPROPYL ALCOHOL
WATER
BENZOCAINE
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
44224-3623	44224-3623-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BENZOCAINE	U3RSY48JW5	ACTIB
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

Source Document#

Source XML

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2a481aa3-562f-dacc-e063-6394a90a32cc			d3afbdea-744a-817b-e053-2995a90ac2d8	2024-12-27	Warnings	Exact identifier spl set id: d3afbdea-744a-817b-e053-2995a90ac2d8

Reported adverse events (FAERS/openFDA)#

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