Hua Tuo

Manufacturer
Wah Ning Pharmaceutical (International) Limited | GUANGZHOU BAIYUNSHAN JINGXIUTANG PHARMACEUTICAL COMPANY
Effective date
2019-10-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:01:22

Label at a glance#

ProductHua Tuo Medicated Plaster Extra Strength
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure11 sections

Indications and uses

For the temporary relief of minor pains and aches of muscles and joints associated with ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Dosage and administration

■ Adults and children 12 years of age and older remove the clear film backing and apply to affected area not more than 3 to 4 times daily ■ Children under 12 years of age, consult a doctor before using. ■ Use caution when applying to hairy skin areas, highly adhesive plaster can hurt when removing.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 3%
Camphor10%

Purpose

OTC - PURPOSE SECTION

External Analgesic

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor pains and aches of muscles and joints associated with ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Warnings

WARNINGS SECTION

For external use only ■ Do not use ■ do not apply to wounds or damaged skin

■ discontinue use if excessive irritation of the skin develops ■ condition affect children uner 12 years of age

When using this product

OTC - WHEN USING SECTION

■ Avoid contact with the eyes or mucus membranes ■ do not bandage tightly ■ Do not use otherwise than as directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

■ redness is present

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a doctor or Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

■ Adults and children 12 years of age and older remove the clear film backing

and apply to affected area not more than 3 to 4 times daily

■ Children under 12 years of age, consult a doctor before using.

■ Use caution when applying to hairy skin areas, highly adhesive plaster can

hurt when removing.

Other Information

SPL UNCLASSIFIED SECTION

■ Store at 68-77ºF (20-25C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

angelica dahurica root, angelica pubescens root, boswellia sacra whole, carthamus tinctorius flower, cinnamon oil, clove oil, commiphora africana resin, drynaria fortunei root, eleutherococcus nodiflorus root bark, ginger, glechoma longituba whole, panax notoginseng root, saposhnikovia divaricata root, schizonepeta tenuifolia flowering top

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1537783camphor 10 % / menthol 3 % Medicated PatchPSN2
1537783camphor 0.1 MG/MG / menthol 0.03 MG/MG Medicated PatchSCD2
1537783camphor 10 % / menthol 3 % Medicated PatchSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73412-001-052021-01-29C16284748780-1ba0f9c33-1569-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73412-001-05Hua TuoMedicated Plaster Extra Strength5 in 1 BOXPATCH52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73412-001HUA TUO MEDICATED PLASTER EXTRA STRENGTH (MENTHOL CAMPHOR) PATCH [WAH NING PHARMACEUTICAL (INTERNATIONAL) LIMITED]2Legacy NDC, 1 package rows20191101_96261180-834d-e3a7-e053-2995a90ad201.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73412-00173412-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
963bced6-196e-fed8-e053-2a95a90accac96261180-834d-e3a7-e053-2995a90ad2012019-10-31WarningsExact identifier
spl id: 963bced6-196e-fed8-e053-2a95a90accac
spl set id: 96261180-834d-e3a7-e053-2995a90ad201

Reported adverse events (FAERS/openFDA)#

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