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: Chattem, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 5767362c-83af-494e-a815-a13f2cb093ef
SPL ID: a4548a1b-2745-42ed-ba2f-38c865f13cd4
Version: 3
Effective date: 2026-01-14
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:45:33

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		Chattem, Inc.	openfda.manufacturer_name
ndc	package	41167-0529-0	openfda.package_ndc
ndc	product	41167-0529	openfda.product_ndc
ndc11	package	41167052900	derived:openfda.package_ndc
rxcui		1010895	openfda.rxcui
spl id		a4548a1b-2745-42ed-ba2f-38c865f13cd4	id
spl set id		5767362c-83af-494e-a815-a13f2cb093ef	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 or blistered areas ■ on deep or puncture wounds When using this product ■ use only as directed. Read and follow all directions and warnings on this label. ■ 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 immediately.

Reported adverse events (FAERS/openFDA)#

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