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NDC 69070-0001-05 Shao Lin Pain Relief Plaster .5; .5 g/100g; g/100g Details

Shao Lin Pain Relief Plaster .5; .5 g/100g; g/100g

Shao Lin Pain Relief Plaster is a TRANSDERMAL PLASTER in the HUMAN OTC DRUG category. It is labeled and distributed by Zhejiang Dingtai Pharmaceutical Co.; Ltd. The primary component is MENTHOL; METHYL SALICYLATE.

Product Information

NDC	69070-0001
Product ID	69070-001_7716374a-a783-4389-8366-8d491224f94e
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Shao Lin Pain Relief Plaster
Proprietary Name Suffix	n/a
Non-Proprietary Name	Menthol, Methyl Salicylate
Product Type	HUMAN OTC DRUG
Dosage Form	PLASTER
Route	TRANSDERMAL
Active Ingredient Strength	.5; .5
Active Ingredient Units	g/100g; g/100g
Substance Name	MENTHOL; METHYL SALICYLATE
Labeler Name	Zhejiang Dingtai Pharmaceutical Co.; Ltd
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part348
Listing Certified Through	2022-12-31

Package

Package Images

NDC 69070-0001-05 (69070000105)

Pricing Information	N/A
NDC Package Code	69070-001-05
Billing NDC	69070000105
Package	5 PATCH in 1 BOX (69070-001-05) / 1 g in 1 PATCH
Marketing Start Date	2010-05-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL f1139b34-4b52-4e72-8a55-02eb3dd8ce8c Details

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: [email protected]

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	05/01/2010

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

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

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

Revised: 10/2021

Document Id: 7716374a-a783-4389-8366-8d491224f94e

Set id: f1139b34-4b52-4e72-8a55-02eb3dd8ce8c

Version: 32747

Effective Time: 20211019