LK HERBAL PATCH- l-menthol patch

LK Herbal Patch by

Drug Labeling and Warnings

LK Herbal Patch 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 5.1%

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: cut plaster to ideal size, remove clear film and apply to affected area
• Avoid over 8 hours of continuous usage or consult your physician
• Do not apply on extermely hairy skin
• Wet the patch with warm water before removing
• 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 CARMICHAELII ROOT, Cao Wu (ACONITUM KUSNEZOFFII LEAF), Di Huang - Radix Rehmanniae, Bai Lian AMPELOPSIS JAPONICA TUBER, Bai Zhi - ANGELICA DAHURICA ROOT, Dang Gui (ANGELICA SINENSIS ROOT), Chi Shao whole PAEONIA LACTIFLORA WHOLE, Qiang Huo whole (HANSENIA FORBESII WHOLE, Wu Yao - LINDERA AGGREGATA ROOT, Gan Cao (LICORICE), Du Huo (ANGELICA PUBESCENS ROOT), Xuan Shen (SCROPHULARIA NINGPOENSIS ROOT), Da Huang ( RHEUM OFFICINALE ROOT), Liu Zhi (SOLIDAGO VIRGAUREA FLOWERING TOP, Methyl salicylate

Product label

INGREDIENTS AND APPEARANCE

LK HERBAL PATCH 
l-menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85954-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	5.1 g

Inactive Ingredients
Ingredient Name	Strength
ACONITUM CARMICHAELII ROOT (UNII: XJ28061U1S)
ACONITUM KUSNEZOFFII LEAF (UNII: SXZ33Q1M29)
REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
AMPELOPSIS JAPONICA TUBER (UNII: O2672197TF)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
PAEONIA LACTIFLORA WHOLE (UNII: N44H57P7WG)
HANSENIA FORBESII WHOLE (UNII: GE02RM96WK)
LINDERA AGGREGATA ROOT (UNII: 517Q7XRT2T)
LICORICE (UNII: 61ZBX54883)
ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ)
SCROPHULARIA NINGPOENSIS ROOT (UNII: HC0FB6P85R)
RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
METHYL SALICYLATE (UNII: LAV5U5022Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85954-002-01	10 in 1 PACKAGE; 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)