WEN TONG GAO- l-menthol ointment

Wen Tong Gao by

Drug Labeling and Warnings

Wen Tong Gao by is a Otc medication manufactured, distributed, or labeled by CAI Industries Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol 15%

Purpose

External analgesic

Uses

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

Warnings

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.

KEEP OUT OF REACH OF CHILDREN

Directions

• 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

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

Inactive ingredients

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

INGREDIENTS AND APPEARANCE

WEN TONG GAO 
l-menthol ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85954-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ACONITUM CARMICHAELII ROOT (UNII: XJ28061U1S)
REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
PAEONIA LACTIFLORA WHOLE (UNII: N44H57P7WG)
LINDERA AGGREGATA ROOT (UNII: 517Q7XRT2T)
ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ)
RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
CHINESE CINNAMON (UNII: WS4CQ062KM)
ACONITUM KUSNEZOFFII LEAF (UNII: SXZ33Q1M29)
AMPELOPSIS JAPONICA TUBER (UNII: O2672197TF)
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
HANSENIA FORBESII WHOLE (UNII: GE02RM96WK)
LICORICE (UNII: 61ZBX54883)
SCROPHULARIA NINGPOENSIS ROOT (UNII: HC0FB6P85R)
MENTHOL, (+)- (UNII: C6B1OE8P3W)
MYRRH (UNII: JC71GJ1F3L)
METHYL SALICYLATE (UNII: LAV5U5022Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85954-003-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	07/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/23/2025

Labeler - CAI Industries Corp. (859060303)