LIGHTS Instant Sting Relief Pad

Manufacturer: Lights Medical Manufacture Co., Ltd.
Effective date: 2026-01-21
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:34:24

Label at a glance#

ProductLIGHTS Instant Sting Relief Pad

Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL

Label structure10 sections

Dosage and administration

For adults and children 2 yeas of age or older: Apply to affected area not more than 3-4 times daily Children under 2 yeas of age: Consult a doctor before use

Storage and handling

Store at room temperature 15-30 C (59-86F). Avoid excessive heat.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6% w/v

Isopropyl Alcohol: 65.4% v/v

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Antiseptic

INDICATIONS & USAGE SECTION

Uses: For temporary relief of pain and itching associated with minor burns, sunburns, minor cut, scrapes, insect bites, or minor skin irritations

WARNINGS SECTION

Warnings:

For external use only. Flammable, keep away from fire or flame. Avoid contact with eyes, if this happens, rinse throughly with water. DO NOT USE with electrocautery procedures.

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or redness develops
if condition worsens or persists for more than 7 days, or clear up and occur again within a few days, consult a physician

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children 2 yeas of age or older: Apply to affected area not more than 3-4 times daily

Children under 2 yeas of age: Consult a doctor before use

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature 15-30 C (59-86F). Avoid excessive heat.

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2700214	benzocaine 6 % / isopropyl alcohol 65.4 % Medicated Pad	PSN	3
2700214	benzocaine 60 MG/ML / isopropyl alcohol 0.654 ML/ML Medicated Pad	SCD	3
2700214	benzocaine 6 % / isopropyl alcohol 65.4 % Medicated Pad	SY	3

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
61333-215-01	LIGHTS Instant Sting Relief Pad	0.8 mL in 1 PATCH	SOLUTION	0.8		3
61333-215-01	LIGHTS Instant Sting Relief Pad	100 in 1 BOX	SOLUTION	100		3

Products#

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

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

LIGHTS Instant Sting Relief Pad
BENZOCAINE
WATER
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61333-215	61333-215-01

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
LIGHTS Instant Sting Relief Pad	BENZOCAINE	Lights Medical Manufacture Co., Ltd.	28dd82a7-f360-a022-e063-6394a90a3a76	2026-01-21	Warnings	Exact identifier ndc (package): 61333-215-01 ndc (product): 61333-215 ndc11 (package): 61333021501 spl id: 48f00055-6bfc-d0c1-e063-6294a90adfb6 spl set id: 28dd82a7-f360-a022-e063-6394a90a3a76

Reported adverse events (FAERS/openFDA)#

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