Shingles Pain Relief Cream

Manufacturer
Hangzhou Jiexiang Technology Co., Ltd
Effective date
2023-02-24
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
legacy-cache
Hydrated at
2026-08-01 21:35:34

Label at a glance#

ProductShingles Pain Relief Cream
Active ingredientWORMWOOD
Label structure12 sections

Dosage and administration

Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream.

Storage and handling

Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream.

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

WHEN USING SECTION

OTC - WHEN USING SECTION

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

STOP USE section

OTC - STOP USE SECTION

condition worsens or does notimprove after regular use asdirected

ASK DOCTOR

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if you are allergic to ingredientsin this product.

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION SECTION

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

Directions

STORAGE AND HANDLING SECTION

Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream.

Other information

INACTIVE INGREDIENT SECTION

Store at room temperature andout of direct sunlight

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​​81991-003-01 Bottle ​81991-003-01 Bottle​81991-003-01 Bottle

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81991-00381991-003-01

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f7b4c9bf-6408-0784-e053-6294a90ac25ef57e1b79-f5ea-ee52-e053-2995a90ab3d82023-03-25WarningsExact identifier
spl set id: f57e1b79-f5ea-ee52-e053-2995a90ab3d8

Reported adverse events (FAERS/openFDA)#

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