SHINGLES PAIN RELIEF CREAM- roycederm shingles pain relief cream cream

Shingles Pain Relief Cream by

Drug Labeling and Warnings

Shingles Pain Relief Cream by is a Otc medication manufactured, distributed, or labeled by Ehy Holdings LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Artemisia extract [fhfi] 3%

Purpose

for shingles skin care

Use

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

Warnings

FOR EXTERNAL USE ONLY

Do not use

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

WHEN USING

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

STOP USE

condition worsens or does notimprove after regular use asdirected

KEEP OUT OF REACH OF CHILDREN

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

Directions

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

Store at room temperature andout of direct sunlight

Inactive ingredients

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

ASK DOCTOR

if you are allergic to ingredientsin this product.

QUESTIONS

Visit www.roycederm.com

Package Label - Principal Display Panel

81799-009-01

INGREDIENTS AND APPEARANCE

SHINGLES PAIN RELIEF CREAM 
roycederm shingles pain relief cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81799-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV)	WORMWOOD	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
WATER (UNII: 059QF0KO0R)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
SMILAX GLABRA WHOLE (UNII: H51N91QNEB)
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81799-009-01	60 g in 1 BOTTLE; Type 0: Not a Combination Product	02/15/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/15/2023

Labeler - Ehy Holdings LLC (117322715)

Establishment
Name	Address	ID/FEI	Business Operations
Ehy Holdings LLC		117322715	manufacture(81799-009)