FDA.reportPublic FDA data

Sting Relief Prep Pad

Manufacturer
NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | Lights Medical Manufacture Co., Ltd.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:32:24

Label at a glance#

ProductSting 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2197238benzocaine 10 % Medicated PadPSN6
2197238benzocaine 100 MG/ML Medicated PadSCD6
2197238benzocaine 10 % Medicated PadSY6

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
73288-004-012023-03-01C16284748780-1ba0f9c33-473d-a910-e053-dadaa90a0b8573288-004
73288-004-012023-01-30C16284748780-1ba0f9c33-473d-a910-e053-dadaa90a0b8573288-004
73288-004-012021-04-28C16284748780-1ba0f9c33-473d-a910-e053-dadaa90a0b8573288-004
73288-004-012021-01-29C16284748780-1ba0f9c33-473d-a910-e053-dadaa90a0b8573288-004

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73288-004-01Sting Relief Prep Pad0.4 g in 1 PATCHSOLUTION0.46
73288-004-01Sting Relief Prep Pad2 in 1 PACKETSOLUTION26

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73288-00473288-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
Sting Relief Prep PadBENZOCAINENINGBO TIANBO FIRST AID PRODUCT CO., LTD.0c901f64-6890-45c0-9ca7-ee9de87903c42026-01-12WarningsExact identifier
ndc (package): 73288-004-01
ndc (product): 73288-004
ndc11 (package): 73288000401
spl id: 483a0737-144c-26d6-e063-6394a90aee39
spl set id: 0c901f64-6890-45c0-9ca7-ee9de87903c4

Reported adverse events (FAERS/openFDA)#

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