Gold Bond Medicated Pain and Itch Relief

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: Gold Bond Medicated Pain and Itch Relief
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: Gold Bond Co LLC
Product type: HUMAN OTC DRUG
SPL set ID: d240e9b8-3506-42ab-8a50-05e8d3fac4ff
SPL ID: 435fea95-2fac-4079-8360-cd156d52a3ba
Version: 1
Effective date: 2025-12-04
Source export date: 2026-10-30
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:21:28

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Gold Bond Medicated Pain and Itch Relief	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Gold Bond Co LLC	openfda.manufacturer_name
ndc	package	84714-0529-0	openfda.package_ndc
ndc	product	84714-0529	openfda.product_ndc
ndc11	package	84714052900	derived:openfda.package_ndc
rxcui		1010895	openfda.rxcui
spl id		435fea95-2fac-4079-8360-cd156d52a3ba	id
spl set id		d240e9b8-3506-42ab-8a50-05e8d3fac4ff	set_id
unii		V13007Z41A	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

Warnings For external use only Do not use in large quantities, particularly over raw surfaces of blistered area on deep or puncture wounds When using this product use only as directed. Read and follow all directions and warnings on this carton. avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days 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.