First Aid Only Sting Relief Pad

Manufacturer: Acme United Corporation
Effective date: 2019-04-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:26:34

Label at a glance#

ProductFirst Aid Only Sting Relief Pad

Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL

Label structure8 sections

Storage and handling

Other Information Store at room temperature

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine, 6% w/v

Isopropyl Alcohol 60% w/v

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Antiseptic

INDICATIONS & USAGE SECTION

Use

For the temporary relief of pait and itching associated with minor burns, scrapes and insect bites. First aid to help prevent infection in minor cuts, scrapes, and burns

DOSAGE & ADMINISTRATION SECTION

Directions

▪adults and children 2 years of age or older, apply to affected area not more than 3 to 4 times daily

▪children under 2 years: consult a physician

WARNINGS SECTION

Warnings

For external use only

Flammable, keep away from fire or flames

OTC - DO NOT USE SECTION

Do not use

In the eyes. If contact occurs, rinse thoroughly with water
over large areas of the body

OTC - STOP USE SECTION

Stop use

If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

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.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Purified Water

STORAGE AND HANDLING SECTION

Other Information

Store at room temperature

Principal Display Panel - 0.4 mL Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0.4 mL Pouch Label 0.4 mL Pouch Label

Products#

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

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

First Aid Only Sting Relief Pad
BENZOCAINE
WATER
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0924-5203	0924-5203-01, 0924-5203-02, 0924-5203-03, 0924-5203-04
65517-0005

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
256a0b9e-0a5b-50cf-e063-6294a90a358f			85dec352-6cac-03fa-e053-2a91aa0a8715	2024-10-26	Warnings	Exact identifier spl set id: 85dec352-6cac-03fa-e053-2a91aa0a8715
DUKAL STING RELIEF PAD	BENZOCAINE	Dukal LLC	67c1ddc7-8fde-4431-84cb-f757682d5f3e	2023-10-13	Warnings	Exact identifier ndc (product): 65517-0005

Reported adverse events (FAERS/openFDA)#

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