SHINGLES PAIN RELIEF CREAM- roycederm shingles pain relief cream ointment
Hangzhou Jiexiang Technology Co., Ltd

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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81991-003
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

WHEN USING SECTION

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

STOP USE section

condition worsens or does notimprove after regular use asdirected

ASK DOCTOR

if you are allergic to ingredientsin this product.

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.

Other information

Store at room temperature andout of direct sunlight

81991-003-01 Bottle

SHINGLES PAIN RELIEF CREAM
roycederm shingles pain relief cream ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81991-003
Route of Administration	CUTANEOUS

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81991-003-01	60 g in 1 BOTTLE; Type 0: Not a Combination Product	02/28/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		02/28/2023	03/02/2023

Labeler - Hangzhou Jiexiang Technology Co., Ltd (699294784)

Name	Address	ID/FEI	Business Operations
Establishment
Hangzhou Jiexiang Technology Co., Ltd		699294784	manufacture(81991-003)

Revised: 3/2023

Document Id: f7b4c9bf-6408-0784-e053-6294a90ac25e

Set id: f57e1b79-f5ea-ee52-e053-2995a90ab3d8

Version: 10

Effective Time: 20230325

Hangzhou Jiexiang Technology Co., Ltd

81991-003 Shingles Pain Relief Cream