Sulfur 8 Kids Anti-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: Sulfur 8 Kids Anti-Dandruff
Generic name: PYRITHIONE ZINC
Manufacturer: J. Strickland & Co.
Product type: HUMAN OTC DRUG
SPL set ID: 89f4ecc8-7a49-42cb-b85d-71c9299e6712
SPL ID: 43046139-7c7e-48eb-e063-6294a90a997b
Version: 3
Effective date: 2025-11-07
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:05:13

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		Sulfur 8 Kids Anti-Dandruff	openfda.brand_name
generic name		PYRITHIONE ZINC	openfda.generic_name
manufacturer name		J. Strickland & Co.	openfda.manufacturer_name
ndc	package	12022-023-00	openfda.package_ndc
ndc	product	12022-023	openfda.product_ndc
ndc11	package	12022002300	derived:openfda.package_ndc
rxcui		209884	openfda.rxcui
spl id		43046139-7c7e-48eb-e063-6294a90a997b	id
spl set id		89f4ecc8-7a49-42cb-b85d-71c9299e6712	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 Ask a doctor before use if you have seborrheic dermatitis that covers a large area of the body. When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and consult a doctor if conditions 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 call a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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