Shingles Pain Relief Cream

Manufacturer: Ehy Holdings LLC
Effective date: 2023-02-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:54:16

Label at a glance#

ProductShingles Pain Relief Cream

Active ingredientWORMWOOD

Label structure14 sections

Dosage and administration

Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream. Apply it 2-3 times a day for thebest result.

Storage and handling

Store at room temperature andout of direct sunlight

Contacts and useful links#

PhonePoison Help1-800-222-1222

Websitewww.roycederm.com

www.roycederm.com

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Artemisia extract [fhfi] 3%

Purpose

OTC - PURPOSE SECTION

for shingles skin care

Use

INDICATIONS & USAGE SECTION

For the treatment of symptomsof shingles, hives, and rashes.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

Do not use

OTC - DO NOT USE SECTION

it on pregnant womenand children under 12 years ofage unless directed by a doctor

OTC - WHEN USING SECTION

avoid contact with eyeslf contact occurs, rinse the eyesthoroughly with water.

OTC - STOP USE SECTION

condition worsens or does notimprove after regular use asdirected

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, getmedical help or contact aPoison Control Center(1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream.
Apply it 2-3 times a day for thebest result.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature andout of direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sophora Flavescens Root,Cnidium Monnieri Fruit, KochiaScoparia Pollen, Dictamnus Dasyca-rpus Root, Smilax Glabra Whole

OTC - ASK DOCTOR SECTION

if you are allergic to ingredientsin this product.

OTC - QUESTIONS SECTION

Visit www.roycederm.com

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

81799-009-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81799-009-01	2024-07-30	C162847	48780-1	1030e365-10c7-111a-e063-dadaa90a10e2	81799-009 Shingles Pain Relief Cream
81799-009-01	2024-01-30	C162847	48780-1	1030e365-10c7-111a-e063-dadaa90a10e2	81799-009 Shingles Pain Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81799-009-01	Shingles Pain Relief Cream	60 g in 1 BOTTLE	CREAM	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81799-009	SHINGLES PAIN RELIEF CREAM (ROYCEDERM SHINGLES PAIN RELIEF CREAM) CREAM [EHY HOLDINGS LLC]	1	1 package rows	20230225_f57d6b13-3b87-5204-e053-2a95a90acee8.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Shingles Pain Relief Cream
RoyceDerm Shingles Pain Relief Cream
DICTAMNUS DASYCARPUS ROOT
WATER
SOPHORA FLAVESCENS ROOT
SMILAX GLABRA WHOLE
CNIDIUM MONNIERI FRUIT
BASSIA SCOPARIA POLLEN
WORMWOOD

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81799-009	81799-009-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DICTAMNUS DASYCARPUS ROOT	6153LEN214	IACT
WATER	059QF0KO0R	IACT
SOPHORA FLAVESCENS ROOT	IYR6K8KQ5K	IACT
SMILAX GLABRA WHOLE	H51N91QNEB	IACT
CNIDIUM MONNIERI FRUIT	V1IA3S3CUS	IACT
BASSIA SCOPARIA POLLEN	07A108ZKW5	IACT
WORMWOOD	F84709P2XV	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f57d6b13-3b88-5204-e053-2a95a90acee8			f57d6b13-3b87-5204-e053-2a95a90acee8	2023-02-24	Warnings	Exact identifier spl id: f57d6b13-3b88-5204-e053-2a95a90acee8 spl set id: f57d6b13-3b87-5204-e053-2a95a90acee8

Reported adverse events (FAERS/openFDA)#

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