Gold Bond Medicated Anti-Itch

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 Anti-Itch
Generic name: PRAMOXINE HYDROCHLORIDE, MENTHOL
Manufacturer: Gold Bond Co LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4a2bd277-47dd-4ae6-9b4b-e0ae9aad226b
SPL ID: 40fadefc-707b-4832-8aa6-00d76ac68cbd
Version: 1
Effective date: 2025-12-05
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:21

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		M017	openfda.application_number
brand name		Gold Bond Medicated Anti-Itch	openfda.brand_name
generic name		PRAMOXINE HYDROCHLORIDE, MENTHOL	openfda.generic_name
manufacturer name		Gold Bond Co LLC	openfda.manufacturer_name
ndc	package	84714-0507-0	openfda.package_ndc
ndc	product	84714-0507	openfda.product_ndc
ndc11	package	84714050700	derived:openfda.package_ndc
rxcui		1293905	openfda.rxcui
spl id		40fadefc-707b-4832-8aa6-00d76ac68cbd	id
spl set id		4a2bd277-47dd-4ae6-9b4b-e0ae9aad226b	set_id
unii		L7T10EIP3A	openfda.unii
unii		88AYB867L5	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 When using this product ■ 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.