LEGERE LAVENDAR FOOT PATCH- topical starch patch

Legere Lavendar Foot Patch by

Drug Labeling and Warnings

Legere Lavendar Foot Patch by is a Otc medication manufactured, distributed, or labeled by Myriad Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Skin Protectant

Uses

May help relieve minor aches and pain

Active Ingredient

Warnings

For external use only / Don’t eat or swallow it

Warnings

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

When using this product

■ Do not use otherwise than directed.

■ Do not stretch out the adhesive tape.

■ Do not take out the contents from the patch.

■ If the patch has been ripped, discard it immediately.

Stop use and ask a doctor if

■ If allergic reaction or irritation occurs

■ If you are pregnant, nursing or under medial treatment

Warnings

■ On wounds, damaged skin, or face.

■ If you are allergic to any ingredients of this product.

■ With, or at the same time as, other external products.

Inactive Ingredients

Bamboo vinegar, Tourmaline, Eucalyptus oil, Mugwort extract, Loquat extract, Vitamin C, Highly purified silica, Perlite, Polyhydric alcohol

directions

Adults and children 4 years of age and over:

Step 1: Clean and dry area for the patch to be attached.

Step 2: Remove the protective cover sheet and gently apply.

Step 3: Leave it on at least 4hours before remove.

Children under 4years of age: Consult with a doctor.

Légère lavender Foot Patch

82504-104-01

INGREDIENTS AND APPEARANCE

LEGERE LAVENDAR FOOT PATCH 
topical starch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82504-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STARCH, CORN (UNII: O8232NY3SJ) (STARCH, CORN - UNII:O8232NY3SJ)	STARCH, CORN	31.92 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)
PYROLIGNEOUS ACID (UNII: N4G9GAT76C)
ERIOBOTRYA JAPONICA LEAF (UNII: Z02066SV11)
PERLITE (UNII: 0SG101ZGK9)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
EUCALYPTUS OIL (UNII: 2R04ONI662)
POLIGLUSAM (UNII: 82LKS4QV2Y)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
SCHORL TOURMALINE (UNII: 173O8XLY6T)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82504-104-01	40 g in 1 BOX; Type 0: Not a Combination Product	01/10/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/10/2022

Labeler - Myriad Co., Ltd. (695004202)

Registrant - Myriad Co., Ltd. (695004202)

Establishment
Name	Address	ID/FEI	Business Operations
Myriad Co., Ltd.		695004202	manufacture(82504-104)