MOISTURIZING DANDRUFF 1% Pyrithione Zinc

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
MOISTURIZING DANDRUFF 1% Pyrithione Zinc
Generic name
PYRITHIONE ZINC
Manufacturer
Bentley Laboratories, LLC
Product type
HUMAN OTC DRUG
SPL set ID
c38b3a45-87f4-4121-8ae6-0a20f7c16c72
SPL ID
45ffb481-0a30-b663-e063-6294a90acd45
Version
3
Effective date
2025-12-15
Source export date
2026-09-28
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/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:38:30
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings : For external use only . Avoid contact with eyes. If contact occurs, rinse Eyes thoroughly with water. If condition worsens or does not improve after regular use of this product as directed, consult a doctor.

Reported adverse events (FAERS/openFDA)#

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