RoyceDerm Rosacea Relief 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: RoyceDerm Rosacea Relief Cream.
Generic name: SULFUR 1X HPUS 10%
Manufacturer: RoyceDerm LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4c3f6332-de46-f107-e063-6294a90ad63f
SPL ID: 4c3f6332-de47-f107-e063-6294a90ad63f
Version: 1
Effective date: 2026-03-04
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:55:45

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M006	openfda.application_number
brand name		RoyceDerm Rosacea Relief Cream.	openfda.brand_name
generic name		SULFUR 1X HPUS 10%	openfda.generic_name
manufacturer name		RoyceDerm LLC	openfda.manufacturer_name
ndc	package	85424-018-01	openfda.package_ndc
ndc	product	85424-018	openfda.product_ndc
ndc11	package	85424001801	derived:openfda.package_ndc
spl id		4c3f6332-de47-f107-e063-6294a90ad63f	id
spl set id		4c3f6332-de46-f107-e063-6294a90ad63f	set_id
unii		70FD1KFU70	openfda.unii

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

For external use only. on damaged or broken skin if you are allergic to sulfur or any of this product's ingredients. avoid contact with eyes do not apply to large areas of skin. Stop use andask a docor if symptomspersist for more than 7 days or worsen. ask a health professional before use. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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