Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner

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 Original Anti-Dandruff Hair and Scalp Conditioner
Generic name: SULFUR
Manufacturer: J. Strickland & Co.
Product type: HUMAN OTC DRUG
SPL set ID: eb1d6e9e-e7fd-478e-80c0-3a3f529682d7
SPL ID: 0834c116-5125-932d-e063-6394a90a13ac
Version: 4
Effective date: 2023-10-21
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 05:56:50

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M032	openfda.application_number
brand name		Sulfur 8 Original Anti-Dandruff Hair and Scalp Conditioner	openfda.brand_name
generic name		SULFUR	openfda.generic_name
manufacturer name		J. Strickland & Co.	openfda.manufacturer_name
ndc	package	12022-017-01	openfda.package_ndc
ndc	package	12022-017-00	openfda.package_ndc
ndc	package	12022-017-02	openfda.package_ndc
ndc	product	12022-017	openfda.product_ndc
ndc11	package	12022001700	derived:openfda.package_ndc
ndc11	package	12022001701	derived:openfda.package_ndc
ndc11	package	12022001702	derived:openfda.package_ndc
rxcui		244368	openfda.rxcui
spl id		0834c116-5125-932d-e063-6394a90a13ac	id
spl set id		eb1d6e9e-e7fd-478e-80c0-3a3f529682d7	set_id
unii		70FD1KFU70	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 eyes throughly with water. Stop use and ask a doctor if condition worsens or does not improve after regular use. Keep out of reach of children If swallower, get medical help or call a poison control center at once.

Reported adverse events (FAERS/openFDA)#

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