Dermoia 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: Dermoia Dandruff
Generic name: PYRITHIONE ZINC
Manufacturer: Treasurewise LLC
Product type: HUMAN OTC DRUG
SPL set ID: 7884bd3e-62ab-4fcd-8870-0a941c3feadb
SPL ID: 50095406-028b-71a7-e063-6294a90ae3c2
Version: 1
Effective date: 2026-04-22
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:27:27

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		Dermoia Dandruff	openfda.brand_name
generic name		PYRITHIONE ZINC	openfda.generic_name
manufacturer name		Treasurewise LLC	openfda.manufacturer_name
ndc	package	83524-965-00	openfda.package_ndc
ndc	product	83524-965	openfda.product_ndc
ndc11	package	83524096500	derived:openfda.package_ndc
rxcui		426904	openfda.rxcui
spl id		50095406-028b-71a7-e063-6294a90ae3c2	id
spl set id		7884bd3e-62ab-4fcd-8870-0a941c3feadb	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 the eyes If contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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