FDA.reportPublic FDA data

JIANZE STING RELIEF PADS

Manufacturer
Changzhou Jianze Sanitary Material Co., Ltd.
Effective date
2012-06-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:32:20

Label at a glance#

ProductJIANZE STING RELIEF PADS
Active ingredientBENZOCAINE
Label structure10 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 a physician.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6%

PURPOSE

OTC - PURPOSE SECTION

Skin Protectant

USE:

INDICATIONS & USAGE SECTION

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

WARNINGS:

WARNINGS SECTION

  • For External Use Only
  • Flammable, keep away from 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

In 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 a physician.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Isopropyl Alcohol, Purified Water

JIANZE STING RELIEF PADS 200 COUNT (50666-008-01)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


StingReliefPadsInnerStingReliefPadsInner

StingReliefPadsOuterStingReliefPadsOuter

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043353benzocaine 6 % Medicated PadPSN2
1043353benzocaine 60 MG/ML Medicated PadSCD2
1043353benzocaine 6 % Medicated WipeSY2
1043353benzocaine 6 % Topical SwabSY2

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50666-008-012019-11-13C16284748780-197449f38-d295-f6ea-e053-dbdaa90aa703JIANZE STING RELIEF PADS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50666-008-01JIANZE STING RELIEF PADS200 in 1 BOXLIQUID2002
50666-008-01JIANZE STING RELIEF PADS0.35 g in 1 POUCHLIQUID0.352

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50666-008JIANZE STING RELIEF PADS (BENZOCAINE) LIQUID [CHANGZHOU JIANZE SANITARY MATERIAL CO., LTD.]2Legacy NDC, 2 package rows20120620_15257cb6-648b-4489-adcc-9ed4a248c528.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZOCAINEACTIVE INGREDIENTU3RSY48JW52
BENZOCAINEACTIVE MOIETYU3RSY48JW52
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M4163022
WATERINACTIVE INGREDIENT059QF0KO0R2

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
50666-00850666-008-01

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
BENZOCAINEU3RSY48JW5ACTIB
ISOPROPYL ALCOHOLND2M416302IACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302LOTION, AUGMENTED / TOPICAL2070 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / AURICULAR (OTIC)6 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL / TOPICAL75 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SPONGE / TOPICAL4 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SWAB / TOPICAL43.9 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SOLUTION / TOPICAL40 %w/vExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302TABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / TOPICAL72 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL, METERED / TOPICAL525 mgExact identifier — unii candidate
9 equally ranked IID candidates

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
2043ea3a-4c3a-499d-bfc8-f1664f3ceeeb15257cb6-648b-4489-adcc-9ed4a248c5282012-06-20WarningsExact identifier
spl id: 2043ea3a-4c3a-499d-bfc8-f1664f3ceeeb
spl set id: 15257cb6-648b-4489-adcc-9ed4a248c528

Reported adverse events (FAERS/openFDA)#

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