Careone Medicated 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
Careone Medicated Dandruff
Generic name
SELENIUM SULFIDE
Manufacturer
Retail Business Services, LLC
Product type
HUMAN OTC DRUG
SPL set ID
cb05b9c6-c1bb-b210-e053-2a95a90afaea
SPL ID
50eb28f4-c45c-8101-e063-6294a90ac2f0
Version
5
Effective date
2021-08-26
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:20:11
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. Ask a doctor before use you have seborrheic dermatitis in areas other than the scalp. When using this Product Avoid contact with eyes. If contact occurs, rinse thoroughly with water. For use on color treated or permed hair, rinse thoroughly. Stop use and ask a doctor if Condition worsens or does not improve after regular use of this product as directed. Keep out of reach of children In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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