Sting Relief Pad

Manufacturer: Hubei Chenteng Healthcare Co.,Ltd.
Effective date: 2019-05-29
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-02 00:23:24

Label at a glance#

ProductSting Relief Pad

Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL

Label structure8 sections

Dosage and administration

Apply to affected area 3 or 4 times daily. For adults and children 2 years of age and older.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine, 6%

Isoprophyl Alcohol, 60.0%

Purpose

OTC - PURPOSE SECTION

Topicaln Anesthetic

Antiseptic

Use

INDICATIONS & USAGE SECTION

Prevent infection of minor scrapes and temporary relief of itching of insect bites

WARNINGS SECTION

For External Use Only

Do Not Use in the eyes. If Contact Occurs, rinse thoroughly with water.

Stop Use If irritation, redness or other symptoms develop.

Caution. If swallowed, get medical help or contact a poison control center right away. Consult a doctor if condition persists or gets worse.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area 3 or 4 times daily. For adults and children 2 years of age and older.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water

Package Label:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Sting Relief Pad
Benzocaine,ISOPROPYL ALCOHOL
WATER
BENZOCAINE
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71509-000	71509-000-00

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
8a0961f4-c78b-3032-e053-2995a90a3b46			896fccdb-54b6-4a21-af13-c7f181f0c373	2019-05-29	Warnings	Exact identifier spl id: 8a0961f4-c78b-3032-e053-2995a90a3b46 spl set id: 896fccdb-54b6-4a21-af13-c7f181f0c373

Reported adverse events (FAERS/openFDA)#

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