DUKAL STING RELIEF PAD

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: DUKAL STING RELIEF PAD
Generic name: BENZOCAINE
Manufacturer: Dukal LLC
Product type: HUMAN OTC DRUG
SPL set ID: 67c1ddc7-8fde-4431-84cb-f757682d5f3e
SPL ID: 07a095bb-40f2-8aed-e063-6394a90aba2f
Version: 6
Effective date: 2023-10-13
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:02

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		DUKAL STING RELIEF PAD	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		Dukal LLC	openfda.manufacturer_name
ndc	package	65517-0005-1	openfda.package_ndc
ndc	product	65517-0005	openfda.product_ndc
ndc11	package	65517000501	derived:openfda.package_ndc
rxcui		895749	openfda.rxcui
spl id		07a095bb-40f2-8aed-e063-6394a90aba2f	id
spl set id		67c1ddc7-8fde-4431-84cb-f757682d5f3e	set_id
unii		U3RSY48JW5	openfda.unii
unii		ND2M416302	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Do Not Use In the eyes. If contact occurs, rinse thoroughly with water Stop Use If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse. Caution Flammable Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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