81991-003 Shingles Pain Relief Cream

Shingles Pain Relief Cream by

Drug Labeling and Warnings

Shingles Pain Relief Cream by is a Otc medication manufactured, distributed, or labeled by Hangzhou Jiexiang Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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
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)

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

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

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

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

Revised: 3/2023

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

34390-5

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

Version: 10

Effective Time: 20230325