SHINGLES PAIN RELIEF CREAM- roycederm shingles pain relief cream cream 
Ehy Holdings LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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81799-009
Shingles Pain Relief Cream

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

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

condition worsens or does notimprove after regular use asdirected

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

if you are allergic to ingredientsin this product.

Visit www.roycederm.com

Package Label - Principal Display Panel

81799-009-01

81799-009-01

SHINGLES PAIN RELIEF CREAM 
roycederm shingles pain relief cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81799-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV) WORMWOOD3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81799-009-0160 g in 1 BOTTLE; Type 0: Not a Combination Product02/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/15/2023
Labeler - Ehy Holdings LLC (117322715)
Establishment
NameAddressID/FEIBusiness Operations
Ehy Holdings LLC117322715manufacture(81799-009)

Revised: 2/2023
Document Id: f57d6b13-3b88-5204-e053-2a95a90acee8
Set id: f57d6b13-3b87-5204-e053-2a95a90acee8
Version: 1
Effective Time: 20230224
 
Ehy Holdings LLC