EXTRA STRENGTH HUA TUO MEDICATED PLASTER

Manufacturer
GUANGZHOU BAIYUNSHAN JINGXIUTANG PHARMACEUTICAL COMPANY
Effective date
2013-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:35:58

Label at a glance#

ProductEXTRA STRENGTH HUA TUO MEDICATED PLASTER
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, MENTHYL SALICYLATE, (+/-)-
Label structure13 sections

Storage and handling

Other information ■ keep in a tightly closed container ■ store at 15º to 30º C (59º to 86º F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Camphor 8.3%
Menthol 3.32%
Methyl salicylate 13.84%

OTC - PURPOSE SECTION

Purpose
External analgesic

INDICATIONS & USAGE SECTION

Uses
For the temporary relief of minor aches and pains of muscles and joints
due to: ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

WARNINGS SECTION

Warnings

For external use only

Allergy alert: This product contains natural rubber latex which may cause allergic reactions

OTC - DO NOT USE SECTION

Do not use
■ on irritated or damaged skin ■ on wounds ■ otherwise than as directed

OTC - WHEN USING SECTION

When using this product
■ avoid contact with the eyes or mucous membranes
■ do not bandage tightly
■ avoid placing on extremely hairy areas of skin to avoid irritation upon removing the plaster

OTC - STOP USE SECTION

Stop use and ask a doctor if
■ condition worsens
■ symptoms persist for more than 7 days
■ symptoms clear up and occur again within a few days
■ excessive irritation of the skin develops
■ nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs
■ when using for pain of arthritis:
■ pain persists for more than 10 days ■ redness is present
■ in conditions affecting children under 12 years of age

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning.
If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions
■ adults and children 3 years of age and older: remove the attached film from the plaster. Apply to affected area not more than 3 to 4 times daily
■ children under 3 years of age: consult your physician
■ refer to the above warnings; use otherwise than as directed may be dangerous

STORAGE AND HANDLING SECTION

Other information
■ keep in a tightly closed container
■ store at 15º to 30º C (59º to 86º F)

INACTIVE INGREDIENT SECTION

Inactive ingredients
African basil (Ocimum gratissimum L) herb oil, cinnamon oil, fang feng root, Formosan sweet gum (Liquidambar formosana Hance) Resin,
fragrant angelica root extract, greater galangal root extract, ginger root extract, huo xue dan [Glechoma longituba (Nakai) Kuprian] aerial part,
natural latex rubber, nux vomica (Strychnos nux-vomica L) seed, rosin, safflower flower, and schizonepeta (Schizonepeta tenuifolia Briq.) flowering
aerial part on a cotton pad.

OTC - QUESTIONS SECTION


Questions or comments? (888) 221-3496 M-F 9 am to 5 pm
■ you may also report serious side effects to this phone number

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


EXTERNAL ANALGESIC
NDC 61821-051-01
EXTRA STRENGTH HUA TUO MEDICATED PLASTER
5 Plasters per Carton
Each Plaster 7x10 cm (2.76 x 3.94 in)IMAGE OF CARTONIMAGE OF CARTON

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1429374camphor 8.3 % / menthol 3.32 % / methyl salicylate 13.84 % Medicated PatchPSN1
1429374camphor 0.083 MG/MG / menthol 0.0332 MG/MG / methyl salicylate 0.138 MG/MG Medicated PatchSCD1
1429374camphor 8.3 % / menthol 3.32 % / methyl salicylate 13.84 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61821-051-012019-11-27C16284748780-19855d018-dc6a-cd31-e053-dbdaa90ab51aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61821-051-01EXTRA STRENGTH HUA TUO MEDICATED PLASTER5 in 1 BOXPLASTER51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61821-051EXTRA STRENGTH HUA TUO MEDICATED PLASTER (CAMPHOR, MENTHOL, METHYL SALICYLATE) PLASTER [GUANGZHOU BAIYUNSHAN JINGXIUTANG PHARMACEUTICAL COMPANY]1Legacy NDC, 1 package rows20130709_9b083eb2-8700-421e-9681-146e7089e390.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET1
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
MENTHYL SALICYLATE, (+/-)-ACTIVE INGREDIENT43XOA705ZD1
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET1
MENTHOLACTIVE MOIETYL7T10EIP3A1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
CINNAMON OILINACTIVE INGREDIENTE5GY4I6YCZ1
GINGERINACTIVE INGREDIENTC5529G5JPQ1
GLECHOMA LONGITUBA TOPINACTIVE INGREDIENTD352074L9S1
GREATER GALANGALINACTIVE INGREDIENT7Y64R856MB1
LIQUIDAMBAR FORMOSANA RESININACTIVE INGREDIENT597LBL467J1
NATURAL LATEX RUBBERINACTIVE INGREDIENT2LQ0UUW8IN1
OCIMUM GRATISSIMUM WHOLEINACTIVE INGREDIENT7V3N80T4VS1
ROSININACTIVE INGREDIENT88S87KL8771
SAFFLOWERINACTIVE INGREDIENT4VBL71TY4Y1
SAPOSHNIKOVIA DIVARICATA ROOTINACTIVE INGREDIENT8H84LFK2QD1
SCHIZONEPETA TENUIFOLIA FLOWERING TOPINACTIVE INGREDIENT2FN3BA1MZE1
STRYCHNOS NUX-VOMICA SEEDINACTIVE INGREDIENT269XH139191

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
61821-05161821-051-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 11 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CINNAMON OILCINNAMON OILE5GY4I6YCZPOWDER, DENTIFRICE / DENTALNAExact identifier — unii candidate
6 equally ranked IID candidates
ROSINROSIN88S87KL877TABLET, EXTENDED RELEASE / ORAL8.99 mgExact identifier — unii candidate
3 equally ranked IID candidates
CINNAMON OILCINNAMON OILE5GY4I6YCZSUSPENSION / ORAL0.2 mg/5mlExact identifier — unii candidate
6 equally ranked IID candidates
CINNAMON OILCINNAMON OILE5GY4I6YCZSYRUP / ORAL0.05 mg/5mlExact identifier — unii candidate
6 equally ranked IID candidates
GINGERGINGERC5529G5JPQSYRUP / ORAL0.05 ml/5mlExact identifier — unii candidate
2 equally ranked IID candidates
ROSINROSIN88S87KL877TABLET, COATED / ORAL10 mgExact identifier — unii candidate
3 equally ranked IID candidates
ROSINROSIN88S87KL877CAPSULE / ORALNAExact identifier — unii candidate
3 equally ranked IID candidates
GINGERGINGERC5529G5JPQELIXIR / ORAL10 mg/5mlExact identifier — unii candidate
2 equally ranked IID candidates
CINNAMON OILCINNAMON OILE5GY4I6YCZPASTE, DENTIFRICE / DENTALNAExact identifier — unii candidate
6 equally ranked IID candidates
CINNAMON OILCINNAMON OILE5GY4I6YCZPASTILLE / ORAL4 mgExact identifier — unii candidate
6 equally ranked IID candidates
CINNAMON OILCINNAMON OILE5GY4I6YCZELIXIR / ORAL0.58 mg/5mlExact identifier — unii candidate
6 equally ranked IID candidates

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
a1352d12-4677-4d4e-a91c-bb902edf7dfa9b083eb2-8700-421e-9681-146e7089e3902013-06-17WarningsExact identifier
spl id: a1352d12-4677-4d4e-a91c-bb902edf7dfa
spl set id: 9b083eb2-8700-421e-9681-146e7089e390

Reported adverse events (FAERS/openFDA)#

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