INSECT STING RELIEF

Manufacturer
GFA Production (Xiamen) Co., Ltd.
Effective date
2025-04-30
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:00:10

Label at a glance#

ProductINSECT STING RELIEF
Active ingredientBENZOCAINE, ALCOHOL
Label structure5 sections

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzocaine, 6% w/v

SD alcohol, 60% w/v 

Purpose:

OTC - PURPOSE SECTION

Topical Anesthetic

Anesthetic

Use:

INDICATIONS & USAGE SECTION

For the 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 eyes, on broken skin, deep puncture wounds. If unsual redness, swelling, irritation or other symptoms occur, consult a physician immediately.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Flammable - keep away from fire or flame. Avoid contact with eyes. If this happens, rinse thoroughly with water

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50814-038INSECT STING RELIEF (BENZOCAINE) SWAB [GFA PRODUCTION (XIAMEN) CO., LTD.]7Legacy NDC20250502_6fc709f5-66e1-243e-e053-2991aa0a3c5d.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50814-03850814-038-01, 50814-038-02

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
NameUNIIKind
BENZOCAINEU3RSY48JW5ACTIB
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4350cdcc-4ce8-262a-e063-6394a90a8ac46fc709f5-66e1-243e-e053-2991aa0a3c5d2025-11-11WarningsExact identifier
spl set id: 6fc709f5-66e1-243e-e053-2991aa0a3c5d

Reported adverse events (FAERS/openFDA)#

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