First Aid Only Sting Relief

Manufacturer
Acme United Corporation
Effective date
2024-11-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:38:04

Label at a glance#

ProductFirst Aid Only Sting Relief
Active ingredientBENZOCAINE, MENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 20 percent

Menthol 1 percent

OTC - PURPOSE SECTION

Topical Analgesic

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses

For temporary relief of the pain and itching of

•insect bites and stings

•minor scrapes and burns

WARNINGS SECTION

Warnings

For external use only.

Do not use

•in the eyes •if you are allergic to any of the ingredients

Stop use and ask a doctor if •conditions worsen •symptoms clear up and then recur •the condition persists for more than 7 days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

If swallowed, contact Poison Control 800.222.1222, or a doctor immediately.

DOSAGE & ADMINISTRATION SECTION

Directions If stinger is present, remove carefully if possible.

Adults Reverse cardboard sleeve so swab is visible. With cardboard sleeve on ampile, crush at dot on sleeve.

There will be a "pop" and the swab will become saturated. Apply saturated applicator to the affected area no more than

3 to 4 times daily.

Children under 2 Consult a doctor.

INFORMATION FOR PATIENTS SECTION

Other Information

Store at room temperature.

INACTIVE INGREDIENT SECTION

D&C Green no. 5, D&C yellow no.10, FD&C blue no.1, isopropyl alcohol, polyethylene glycol 300, purified water

OTC - QUESTIONS SECTION

Questions 800.835.2263

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sting Swabs Carton ImageSting Swabs Carton ImageBOX19001-revD (002).jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1037117benzocaine 20 % / menthol 1 % Medicated PadPSN3
1037117benzocaine 200 MG/ML / menthol 10 MG/ML Medicated PadSCD3
1037117benzocaine 20 % / menthol 1 % Topical SwabSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0924-5250-01First Aid Only Sting Relief6 mL in 1 AMPULESWAB63
0924-5250-01First Aid Only Sting Relief10 in 1 CARTONSWAB103
0924-5250-03First Aid Only Sting Relief6 mL in 1 AMPULESWAB63
0924-5250-03First Aid Only Sting Relief100 in 1 CARTONSWAB1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0924-5250FIRST AID ONLY STING RELIEF (BENZOCAINE) SWAB [ACME UNITED CORPORATION]3Current NDC, Legacy NDC, 4 package rows20241121_697127d1-c02e-16d2-e053-2a91aa0a39fd.zip

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
0924-52500924-5250-01, 0924-5250-03
46414-2040

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Medicaine Sting and BiteBENZOCAINEJames Alexander Corporation753e6cbe-31e0-4017-93d0-8b4bf5972f372024-12-09WarningsExact identifier
ndc (product): 46414-2040
First Aid Only Sting ReliefBENZOCAINEAcme United Corporation697127d1-c02e-16d2-e053-2a91aa0a39fd2024-11-19WarningsExact identifier
ndc (package): 0924-5250-01
ndc (package): 0924-5250-03
ndc (product): 0924-5250
ndc11 (package): 00924525003
ndc11 (package): 00924525001
spl id: 27490db9-8f9d-c804-e063-6394a90abbc5
spl set id: 697127d1-c02e-16d2-e053-2a91aa0a39fd

Reported adverse events (FAERS/openFDA)#

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