RoyceDerm Seborrheic Dermatitis and Dandruff Medicated Cleansing Bar

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
RoyceDerm Seborrheic Dermatitis and Dandruff Medicated Cleansing Bar
Generic name
PYRITHIONE ZINC 2%
Manufacturer
RoyceDerm LLC
Product type
HUMAN OTC DRUG
SPL set ID
3b98a83d-9c3b-9522-e063-6294a90a7033
SPL ID
3b98a83d-9c3c-9522-e063-6294a90a7033
Version
1
Effective date
2025-08-05
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:10:22
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only you have a conditionthat covers a large area of the body. avoid contact with eyesIf contact occurs, rinse thoroughly with water. if condition worsensor does not improve. ask a healthprofessional before use. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away.(1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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