Dermgentle Seborrheic Face Cream

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
Dermgentle Seborrheic Face Cream
Generic name
PYRITHIONE ZINC
Manufacturer
Dermgentle LLC
Product type
HUMAN OTC DRUG
SPL set ID
45232668-6953-80a0-e063-6294a90a6e4b
SPL ID
458124b2-bce7-4ea7-e063-6394a90a616e
Version
2
Effective date
2025-12-12
Source export date
2026-10-27
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:46:27
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 product gets into eyes, rinse eyes thoroughly with water. Ask a doctor before use if • condition covers a large area of the body. Do not use • on skin that is broken or inflamed • if you are allergic to ingredients in this product. Stop use and ask a doctor if • rash appears • condition worsens or does not improve after regular use of this product as directed. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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