Glovers Dandruff Control Medicine, Regular

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
Glovers Dandruff Control Medicine, Regular
Generic name
SULFUR
Manufacturer
J. Strickland & Co.
Product type
HUMAN OTC DRUG
SPL set ID
18700036-11ec-4370-bcc6-b9e2c732e7d9
SPL ID
08340897-23b3-f23b-e063-6294a90a4eb9
Version
5
Effective date
2023-10-21
Source export date
2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:09:51
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 do not get into eyes. If contact occurs rinse eyes thoroughly with water. Stop use and consult a doctor if if skin irritation develops or increases. condition worsens or does not improve after regular use. Keep out of reach of children If swallowed, 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.