FDA.reportPublic FDA data

LIGHTS Sting Relief Prep Pad

Manufacturer
Lights Medical Manufacture Co., Ltd.
Effective date
2025-06-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:02:18

Label at a glance#

ProductLIGHTS Sting Relief Prep Pad
Active ingredientBENZOCAINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Benzocaine 10% w/v

OTC - PURPOSE SECTION

Purpose: Topical Anesthetic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings:

For external use only

Do not use: In the eyes, on broken skin, deep puncture wounds. I f unusal redness, swelling, irritation, or other symptoms occur, consult a physician immediately. 

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

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

DOSAGE & ADMINISTRATION SECTION

Directions: Wipe injection site vigorously and discard

INACTIVE INGREDIENT SECTION

Inactive Ingredient

Purified Water, Isopropyl Alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2197238benzocaine 10 % Medicated PadPSN4
2197238benzocaine 100 MG/ML Medicated PadSCD4
2197238benzocaine 10 % Medicated PadSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61333-211-012025-06-05C16284748780-11030e365-426a-111a-e063-dadaa90a10e261333-211 Sting Relief
61333-211-012024-01-30C16284748780-11030e365-426a-111a-e063-dadaa90a10e261333-211 Sting Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61333-211-01LIGHTS Sting Relief Prep Pad100 in 1 BOXSOLUTION1004
61333-211-01LIGHTS Sting Relief Prep Pad0.4 g in 1 PATCHSOLUTION0.44

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
61333-21161333-211-01

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
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
BENZOCAINEU3RSY48JW5ACTIB

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
LIGHTS Sting Relief Prep PadBENZOCAINELights Medical Manufacture Co., Ltd.4f4d7758-be62-4304-8871-087a90497fa52025-06-04WarningsExact identifier
ndc (package): 61333-211-01
ndc (product): 61333-211
ndc11 (package): 61333021101
spl id: 36cbcd22-b303-ebd3-e063-6394a90a2cce
spl set id: 4f4d7758-be62-4304-8871-087a90497fa5

Reported adverse events (FAERS/openFDA)#

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