ITCHY SCALP RELIEF DANDRUFF

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: ITCHY SCALP RELIEF DANDRUFF
Generic name: PYRITHIONE ZINC
Manufacturer: Universal Distribution Center LLC
Product type: HUMAN OTC DRUG
SPL set ID: 634019c2-03a3-4fed-939e-6f9a50ddea7b
SPL ID: b5f4b5be-2e93-467e-bcc7-ce8d7575b9f0
Version: 1
Effective date: 2026-08-24
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:19

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		M032	openfda.application_number
brand name		ITCHY SCALP RELIEF DANDRUFF	openfda.brand_name
generic name		PYRITHIONE ZINC	openfda.generic_name
manufacturer name		Universal Distribution Center LLC	openfda.manufacturer_name
ndc	package	52000-453-12	openfda.package_ndc
ndc	product	52000-453	openfda.product_ndc
ndc11	package	52000045312	derived:openfda.package_ndc
rxcui		1043014	openfda.rxcui
spl id		b5f4b5be-2e93-467e-bcc7-ce8d7575b9f0	id
spl set id		634019c2-03a3-4fed-939e-6f9a50ddea7b	set_id
unii		R953O2RHZ5	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. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation occurs or condition worsens after regular use. 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.