QUALI PATCH HERBAL SOULTICE- menthol, methyl salicylate patch

Quali Patch Herbal Soultice by

Drug Labeling and Warnings

Quali Patch Herbal Soultice by is a Otc medication manufactured, distributed, or labeled by Finemost Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Menthol   10%

Methyl Salicylate   0.5%

Purpose

Menthol         Topical Analgesic

Methyl Salicylate       Topical Analgesic

Uses

For temporary relief of minor aches and pains of muscles and joints associated with:

Simple backache
Arthritis
Sprains
Strains
Bruises

Warnings

1. For external use only. Avoid applying around the eyes and mucous membranes, or open wounds.
2. Pregnant women, nursing mothers and any person with allergic reactions to drugs or cosmetics should consult physician before use. Children should use this product under supervision.

Stop Use

Discontinue if skin irritation develops.

Keep Out Of Reach of Children.

Keep out of reach of children.

Directions

1. Clean and dry the affected areas before application.
2. Remove the protective film while applying the areas 1-2 times daily, cut into smaller size if desired. If necessary up to 3 sheets per day.
3. Use only as directed. Firmly affix with adhesive tapes or elastic bandages around joint areas to secure the patch if needed.

Storage

Store at room temperature away from direct sunlight. Properly sealed to remain fresh.

Inactive Ingredients

ANGELICA SINENSIS ROOT, ANGELICA DAHURICA WHOLE, ALMOND, SCROPHULARIA NINGPOENSIS ROOT, GLEDITSIA SINENSIS WHOLE, LIQUIDAMBAR FORMOSANA RESIN, ALLIUM FISTULOSUM WHOLE, TURPENTINE, FRANKINCENSE, MYRRH, YELLOW WAX, ROSIN, ZINC OXIDE, SESAME OIL

Distributed by

Finemost Corp. DBA Qualiherb

Cerritos, Ca 90703

Tel:   (562)802-0035

Fax: (562)802-0625

Made in Taiwan

Drug Facts

INGREDIENTS AND APPEARANCE

QUALI PATCH HERBAL SOULTICE 
menthol, methyl salicylate patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72026-883
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
ANGELICA DAHURICA WHOLE (UNII: 667W6C5J4P)
ALMOND (UNII: 3Z252A2K9G)
SCROPHULARIA NINGPOENSIS ROOT (UNII: HC0FB6P85R)
GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)
LIQUIDAMBAR FORMOSANA RESIN (UNII: 597LBL467J)
ALLIUM FISTULOSUM WHOLE (UNII: 51BV41D79A)
TURPENTINE (UNII: XJ6RUH0O4G)
FRANKINCENSE (UNII: R9XLF1R1WM)
MYRRH (UNII: JC71GJ1F3L)
YELLOW WAX (UNII: 2ZA36H0S2V)
ROSIN (UNII: 88S87KL877)
ZINC OXIDE (UNII: SOI2LOH54Z)
SESAME OIL (UNII: QX10HYY4QV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72026-883-01	100 in 1 BOX	10/10/2013	10/10/2033
1		16 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/10/2013	10/10/2033

Labeler - Finemost Corporation (623264082)