Sting Relief

Manufacturer: Jianerkang Medical Co., Ltd
Effective date: 2023-10-23
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:57:17

Label at a glance#

ProductSting Relief

Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL

Label structure9 sections

Dosage and administration

Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age or older. Children under 2 years: consult physician.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6%

Isopropyl Alcohol 60% w/v

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Antiseptic

USE

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For External use only
Flammable, keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

In the eyes. If contact occurs, flush eyes with water

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age or older. Children under 2 years: consult physician.

Other information

STORAGE AND HANDLING SECTION

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label - Sting Relief Pads

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
895749	benzocaine 6 % / isopropyl alcohol 60 % Medicated Pad	PSN	4
895749	benzocaine 60 MG/ML / isopropyl alcohol 0.6 ML/ML Medicated Pad	SCD	4
895749	benzocaine 6 % / isopropyl alcohol 60 % Medicated Pad	SY	4
895749	benzocaine 6 % / isopropyl alcohol 60 % Topical Swab	SY	4

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
BENZOCAINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
34645-4190-1	Sting Relief	0.56 g in 1 POUCH	SWAB	0.56		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
34645-4190	STING RELIEF (BENZOCAINE, ISOPROPYL ALCOHOL) SWAB [JIANERKANG MEDICAL CO., LTD]	4	Current NDC, Legacy NDC, 1 package rows	20231023_3a32398a-3f7e-4da0-bb1d-b3f369914b2a.zip

Products#

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

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

Sting Relief
BENZOCAINE, ISOPROPYL ALCOHOL
WATER
BENZOCAINE
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
34645-4190	34645-4190-1

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
Sting Relief	BENZOCAINE, ISOPROPYL ALCOHOL	Jianerkang Medical Co., Ltd	3a32398a-3f7e-4da0-bb1d-b3f369914b2a	2023-10-23	Warnings	Exact identifier ndc (package): 34645-4190-1 ndc (product): 34645-4190 ndc11 (package): 34645419001 spl id: 085bcc1d-8ee9-1348-e063-6394a90af6cf spl set id: 3a32398a-3f7e-4da0-bb1d-b3f369914b2a

Reported adverse events (FAERS/openFDA)#

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