SHAO LIN PAIN RELIEF PLASTER- menthol, methyl salicylate plaster

Shao Lin Pain Relief Plaster by

Drug Labeling and Warnings

Shao Lin Pain Relief Plaster by is a Otc medication manufactured, distributed, or labeled by Zhejiang Dingtai Pharmaceutical Co.; Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol   0.5%

Methyl Salicylate  0.5%

Purpose

Menthol   External Analgesic

Methyl Salicylate     External Analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints due to:

simple backache

arthritis

strains

bruises

sprains

Warning

For External Use Only.

Do Not Use

on wounds

on irritated or damaged skin

if the appearance of this product has changed

in excess of 12 hours

if you have known hypersensitive to this product

otherwise than as directed

Ask a Doctor or Pharmacist Before Use If You Are

pregnant

taking other medications

When Using This Product

avoid contact with the eye or mucous membranes

do not bandage tightly

supervise use by children

use caution if prone to allergic reactions

Stop Use and Ask a Doctor If

condition worsens

symptoms persist for more than 7 days

symptoms clear up and occur again within a few days

excessive irritation of the skin develops

when using for pain of arthritis

pain persists for more than 10 days

redness is present

in conditions affecting children under 12 years of age

Keep Out of Reach of Children.

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

Directions

Adults and children 12 years of age and older: Apply one or two plasters to affected area once a day. Remove after 12 hours.
Children 2 to 12 years of age and adults with compromised health: Use only under the guidance of a doctor.
Children under 2 years of age: Do not use, consult a doctor.
Refer to the above warnings: use otherwise than as directed may be dangerous.

Other Information

Keep container tightly closed.

Store below 20 ℃ (68 ℉) in a dry area.

Inactive Ingredients

PEPPERS, LINDERA AGGREGATA ROOT, BLETILLA STRIATA BULB, ANGELICA DAHURICA ROOT, AMPELOPSIS JAPONICA ROOT, PAWPAW, SPARGANIUM STOLONIFERUM WHOLE, CURCUMA ZEDOARIA LEAF, ANGELICA SINENSIS ROOT, PAEONIA VEITCHII ROOT, CINNAMON, RHEUM PALMATUM WHOLE, FORSYTHIA SUSPENSA WHOLE, DRAGON'S BLOOD, FRANKINCENSE, MYRRH, PANAX NOTOGINSENG ROOT, ACACIA CATECHU WHOLE, BORNEOL

Questions or Comments?

Call (626)350-5000 or

E-mail: upc168@sbcglobal.net

Manufacturerd by

Zhejiang Dingtai Pharmaceutical Co.; Ltd

No. 1392, Huancheng South Road, Economy Development Zone,

Tongxiang, Zhejiang 314500, China

Distributed by

UPC Medical Supplies, Inc.

11030 Weaver Avenue

South El Monte, CA 91733  USA

Drug Facts

INGREDIENTS AND APPEARANCE

SHAO LIN PAIN RELIEF PLASTER 
menthol, methyl salicylate plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69070-001
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.5 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
PEPPERS (UNII: T5KDM4J239)
LINDERA AGGREGATA ROOT (UNII: 517Q7XRT2T)
BLETILLA STRIATA BULB (UNII: 00T5SH6SEJ)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
AMPELOPSIS JAPONICA ROOT (UNII: O2672197TF)
PAWPAW (UNII: 8P95FP65YO)
SPARGANIUM STOLONIFERUM WHOLE (UNII: 873IV8AW3C)
CURCUMA ZEDOARIA LEAF (UNII: M9E9LQH7N4)
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
PAEONIA VEITCHII ROOT (UNII: VX6GD6M93V)
CINNAMON (UNII: 5S29HWU6QB)
RHEUM PALMATUM WHOLE (UNII: 75P857ARCY)
FORSYTHIA SUSPENSA WHOLE (UNII: RO2K2K561Z)
DRAGON'S BLOOD (UNII: M3YJ2C28IC)
FRANKINCENSE (UNII: R9XLF1R1WM)
MYRRH (UNII: JC71GJ1F3L)
PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
ACACIA CATECHU WHOLE (UNII: TJ6XA84OQF)
BORNEOL (UNII: M89NIB437X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69070-001-05	5 in 1 BOX	05/01/2010
1		1 g in 1 PATCH; 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	05/01/2010

Labeler - Zhejiang Dingtai Pharmaceutical Co.; Ltd (420598724)

Registrant - Zhejiang Dingtai Pharmaceutical Co.; Ltd (420598724)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Dingtai Pharmaceutical Co.; Ltd		420598724	manufacture(69070-001)