FDA.reportPublic FDA data

Wen Tong Gao

Manufacturer
CAI Industries Corp.
Effective date
2025-08-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:11:19

Label at a glance#

ProductWen Tong Gao
Active ingredientLEVOMENTHOL
Label structure8 sections

Indications and uses

Temporarily relieves muscle and joint pains: backaches, arthritis, strains, bruises, sprains

Dosage and administration

Adults and children 12 years of age and older : Apply it and massage into affected areas. Children under 12 years of age : consult your physician

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 15%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves muscle and joint pains: backaches, arthritis, strains, bruises, sprains

Warnings

WARNINGS SECTION

For external use only

When using this product 

  • avoid contact with the eyes or mucous membranes 
  • do not use on wounds or broken skin

Stop use and ask a doctor if

  • conditions worsen 
  • excessive skin irritation develops
  • nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash occurs
  • symptoms persists for more than 7 days

If pregnant or breast-feeding, ask a doctor before use.

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12 years of age and older: Apply it and massage into affected areas.
  • Children under 12 years of age: consult your physician

Other Information

SPL UNCLASSIFIED SECTION

  • Keep unused plasters in the pouch
  • Store in a cool dry place at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Chuan Wu (Aconitum Carmichaelli Root), Di Huang (Rehmannia Glutinosa Root), Bai Zhi (Angelica Dahurica Root), Chi Shao (Paeonia Lactiflora Whole), Wu Yao (Lindera Aggregata Root), Du Huo (Angelica Pubescens Root), Da Huang (Rheum Officinale Root), Rou Gui Resin (Chinese Cinnamon), Cao Wu (Aconitum Kusnezoffii Leaf), Bai Lian (Ampelopsis Japonica Tuber), Dang Gui (Angelica Sinensis Root), Qiang Huo (Hansenia Forbsii Whole), Gan Cao (Licorice Root), Xuan Shen (Scrophularia Ningpoensis Root), Mo Yao (Myrrh), Ru Xiang (Frankincense), Methyl Salicylate

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311501menthol 15 % Topical OintmentPSN1
311501menthol 0.15 MG/MG Topical OintmentSCD1
311501menthol 15 % Topical OintmentSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85954-003-01Wen Tong Gao30 g in 1 BOTTLEOINTMENT301

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85954-00385954-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEVOMENTHOLBZ1R15MTK7ACTIB
ACONITUM CARMICHAELII ROOTXJ28061U1SIACT
REHMANNIA GLUTINOSA ROOT1BEM3U6LQQIACT
ANGELICA DAHURICA ROOT1V63N2S972IACT
PAEONIA LACTIFLORA WHOLEN44H57P7WGIACT
LINDERA AGGREGATA ROOT517Q7XRT2TIACT
ANGELICA PUBESCENS ROOT0MF1EI01KJIACT
RHEUM OFFICINALE ROOTA47JP5ZG9MIACT
CHINESE CINNAMONWS4CQ062KMIACT
ACONITUM KUSNEZOFFII LEAFSXZ33Q1M29IACT
AMPELOPSIS JAPONICA TUBERO2672197TFIACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
HANSENIA FORBESII WHOLEGE02RM96WKIACT
LICORICE61ZBX54883IACT
SCROPHULARIA NINGPOENSIS ROOTHC0FB6P85RIACT
MENTHOL, (+)-C6B1OE8P3WIACT
MYRRHJC71GJ1F3LIACT
METHYL SALICYLATELAV5U5022YIACT

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
575dd7b5-2a34-d936-e063-6294a90a10782dcd1db5-8bf1-4296-b280-b4e2012e649c2026-07-24WarningsExact identifier
spl set id: 2dcd1db5-8bf1-4296-b280-b4e2012e649c