Sting Relief

Manufacturer: Yiwu Ori-Power Medtech Co.,Ltd.
Effective date: 2024-01-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 21:12:02

Label at a glance#

ProductSting Relief

Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL

Label structure7 sections

Dosage and administration

Apply to affected area no more than 3 to 4 times daily. For children under 2 years of age, consult physician before use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6% w/v, Isopropyl Alcohol 60% w/v

Purpose

OTC - PURPOSE SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Sodium Bicarbonate.

Use

INDICATIONS & USAGE SECTION

Temporary relief for minor burns, scrapes and insect bites.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area no more than 3 to 4 times daily. For children under 2 years of age, consult physician before use.

Storage

SPL UNCLASSIFIED SECTION

Store at room temperature 15°C - 30°C (59°F - 86°F).

Warnings

WARNINGS SECTION

Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If irritation develops, consult physician. Do not use on broken skin, deep puncture wounds.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental swallowing, seek medical help and contact poison control immediately.

Do not use

OTC - DO NOT USE SECTION

on broken skin, deep puncture wounds.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Sting Relief
BENZOCAINE, ISOPROPYL ALCOHOL
WATER
SODIUM BICARBONATE
BENZOCAINE
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72459-282	72459-282-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM BICARBONATE	8MDF5V39QO	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
33ed2573-e62a-6dc0-e063-6294a90ad270			75f0296c-e121-4276-a7e8-ad1b976ead39	2025-04-29	Warnings	Exact identifier spl set id: 75f0296c-e121-4276-a7e8-ad1b976ead39

Reported adverse events (FAERS/openFDA)#

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