FDA.reportPublic FDA data

Sulfur 8 Scalp Therapy Medicated Dandruff Control

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 Scalp Therapy Medicated Dandruff Control
Generic name
SALICYLIC ACID
Manufacturer
J. Strickland and Co.
Product type
HUMAN OTC DRUG
SPL set ID
961ffab9-4e1b-83f3-e053-2a95a90af5fe
SPL ID
0834eb14-2e95-ef47-e063-6294a90ad922
Version
3
Effective date
2023-10-21
Source export date
2026-08-17
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/2026-08-17/0b1cc8680154603ac269ec69e1c6611714d626104ff688eca4b2c067b511bd72/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 07:48:45
Harmonized routes table
Harmonized routes
TOPICAL

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, rinse eyes thoroughly with water. Stop use and consult 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 call a Poison Control Center at once.