Sulfur 8 Light 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 Light Anti-Dandruff Hair and Scalp Conditioner
Generic name: SULFUR
Manufacturer: J. Strickland & Co.
Product type: HUMAN OTC DRUG
SPL set ID: d8f9afe8-bc44-41be-806b-b77d2def0fb0
SPL ID: 0833fc64-f83f-f3b0-e063-6294a90aeec1
Version: 4
Effective date: 2023-10-21
Source export date: 2026-10-12
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:36:59

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 Light 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	12022-018-01	openfda.package_ndc
ndc	package	12022-018-02	openfda.package_ndc
ndc	package	12022-018-00	openfda.package_ndc
ndc	product	12022-018	openfda.product_ndc
ndc11	package	12022001802	derived:openfda.package_ndc
ndc11	package	12022001801	derived:openfda.package_ndc
ndc11	package	12022001800	derived:openfda.package_ndc
rxcui		244368	openfda.rxcui
spl id		0833fc64-f83f-f3b0-e063-6294a90aeec1	id
spl set id		d8f9afe8-bc44-41be-806b-b77d2def0fb0	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 do not get into 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. If swallowed, get medical help or call a poison control center at once. a gradual blue-black darking of the skin occurs irritation becomes severe no improvement is seen after 3 months

Reported adverse events (FAERS/openFDA)#

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