SHENG CHUN HERBAL

Manufacturer: Sheng Chun Tang Pharmaceutical Industrial Co., Ltd | Albert Max, Inc.
Effective date: 2014-02-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:38:27

Label at a glance#

ProductSHENG CHUN HERBAL Pain Relieving

Active ingredientMENTHOL, METHYL SALICYLATE

Label structure14 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints due to: arthritis strains bruises sprains simple backaches

Dosage and administration

Adults and children 12 years of age and older: clean and dry affected area. Remove patch from the protective layer, apply to the affected area, rub the area with your hand to secure the patch. Patch will remain effective for 8 hours. Avoid using the same patch on the same area for more than 2 days. Do not apply to area with excessive hair. Adhesive patch may hurt skin upon removal. Wet patch with warm water before...

Contacts and useful links#

PhoneLabel contact1-800-617-2021

Label contents#

Full prescribing information#

Drug Facts Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

Methyl Salicylate 1%

Purpose

OTC - PURPOSE SECTION

External analgesic

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning.

In case of overdose, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

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

arthritis
strains
bruises
sprains
simple backaches

Warnings

WARNINGS SECTION

For external use only

Do not use otherwise than as directed.

Do not use

OTC - DO NOT USE SECTION

on wounds
irritated or damaged skin
sensitive skin
with a heating pad
if pregnant
with, or as the same time as other external analgesic products
if allergic to aspirin or salicylates
if allergic to any ingredients of this product

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes
do not bandage tightly
do not apply to wounds or damaged skin
do not use more than 3 plasters a day
do not use 1 hour before or after bathing

Stop use and ask a doctor if

OTC - STOP USE SECTION

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
rashes, itching or redness are present
side effects occur. You may call: 1-800-617-2021

If pregnant,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: clean and dry affected area. Remove patch from the protective layer, apply to the affected area, rub the area with your hand to secure the patch.
Patch will remain effective for 8 hours.
Avoid using the same patch on the same area for more than 2 days.
Do not apply to area with excessive hair. Adhesive patch may hurt skin upon removal.
Wet patch with warm water before removing from skin.
Children under 12 years of age: Do not use or consult a doctor.

Other Information

OTHER SAFETY INFORMATION

Store unused patch in the pouch
Store at room temperature, 20 to 25° C (68 to 77° F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Chinese Clematidis Root and Rhizome, Yellow wax, Momordica cochinchinensis seeds, Castor Seeds, Myrrh, Frankincense, Sesame Oil, Resin, FD and C Blue No. 2, FD and C Yellow No. 4, Zinc Oxide

Questions or comments

OTC - QUESTIONS SECTION

Call 1-800-617-2021

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GMP

"SHENG CHUN" HERBAL PATCH
Pain Relieving Patch

backache arthritis strains bruises sprains

FOR EXTERNAL USE ONLY

Contains 3(11X15cm 4.3inchX5.9inch)Patches

"GREEN PATCH"

For the temporary relief of muscles and joints associated with arthritis

Manufactured by:
SHENG CHUN TANG PHARMACEUTICAL INDUSTRIAL CO., LTD. TAIWAN

Distributed by:
Albert Max
13859 Redwood Ave. Chino, CA 91710 USA

Made in Taiwan

AM ShengChun103 Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1483688	menthol 5 % / methyl salicylate 1 % Medicated Patch	PSN	1
1483688	menthol 0.05 MG/MG / methyl salicylate 0.01 MG/MG Medicated Patch	SCD	1
1483688	menthol 5 % / methyl salicylate 1 % Medicated Patch	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
67473-103-01	2020-01-31	C162847	48780-1	9d75b9d0-4a4a-f424-e053-dadaa90a57ce	d4adaa46-062e-4c1e-9d9c-e7073463a40d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67473-103-01	SHENG CHUN HERBALPain Relieving	3 in 1 BOX	PATCH	3		1
67473-103-01	SHENG CHUN HERBALPain Relieving	4 g in 1 PATCH	PATCH	4		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67473-103	SHENG CHUN HERBAL PAIN RELIEVING (MENTHOL, METHYL SALICYLATE) PATCH [SHENG CHUN TANG PHARMACEUTICAL INDUSTRIAL CO., LTD]	1	Legacy NDC, 2 package rows	20140220_d4adaa46-062e-4c1e-9d9c-e7073463a40d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	1
METHYL SALICYLATE	ACTIVE INGREDIENT	LAV5U5022Y	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	1
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	1
CLEMATIS CHINENSIS ROOT	INACTIVE INGREDIENT	8Z18N528CU	1
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	1
FD&C YELLOW NO. 5	INACTIVE INGREDIENT	I753WB2F1M	1
FRANKINCENSE	INACTIVE INGREDIENT	R9XLF1R1WM	1
MOMORDICA COCHINCHINENSIS SEED	INACTIVE INGREDIENT	2T87O1UPVD	1
MYRRH	INACTIVE INGREDIENT	JC71GJ1F3L	1
PINUS MASSONIANA RESIN	INACTIVE INGREDIENT	64S07U83T7	1
RICINUS COMMUNIS SEED	INACTIVE INGREDIENT	7EK4SFN1TX	1
SESAME OIL	INACTIVE INGREDIENT	QX10HYY4QV	1
YELLOW WAX	INACTIVE INGREDIENT	2ZA36H0S2V	1
ZINC OXIDE	INACTIVE INGREDIENT	SOI2LOH54Z	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

SHENG CHUN HERBAL Pain Relieving
MENTHOL, METHYL SALICYLATE
MENTHOL
METHYL SALICYLATE
SALICYLIC ACID
CLEMATIS CHINENSIS ROOT
YELLOW WAX
MOMORDICA COCHINCHINENSIS SEED
RICINUS COMMUNIS SEED
MYRRH
FRANKINCENSE
SESAME OIL
PINUS MASSONIANA RESIN
FD&C BLUE NO. 2
FD&C YELLOW NO. 5
ZINC OXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
67473-103	67473-103-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
METHYL SALICYLATE	LAV5U5022Y	ACTIB
CLEMATIS CHINENSIS ROOT	8Z18N528CU	IACT
YELLOW WAX	2ZA36H0S2V	IACT
MOMORDICA COCHINCHINENSIS SEED	2T87O1UPVD	IACT
RICINUS COMMUNIS SEED	7EK4SFN1TX	IACT
MYRRH	JC71GJ1F3L	IACT
FRANKINCENSE	R9XLF1R1WM	IACT
SESAME OIL	QX10HYY4QV	IACT
PINUS MASSONIANA RESIN	64S07U83T7	IACT
FD&C BLUE NO. 2	L06K8R7DQK	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
ZINC OXIDE	SOI2LOH54Z	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 50 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	LOZENGE / BUCCAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	TABLET, CHEWABLE / ORAL		3 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SUPPOSITORY / VAGINAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, SUGAR COATED / ORAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	TABLET, DELAYED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	TABLET, FILM COATED / ORAL		2 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	CREAM / TOPICAL	5 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	TABLET / ORAL		25 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	POWDER / TOPICAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	CONCENTRATE / BUCCAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
SESAME OIL	SESAME OIL	QX10HYY4QV	INJECTION / INTRAMUSCULAR	70 %v/v		Exact identifier — unii candidate 2 equally ranked IID candidates
SESAME OIL	SESAME OIL	QX10HYY4QV	CAPSULE / ORAL		2325 mg	Exact identifier — unii candidate 2 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET / ORAL	3.22 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	CAPSULE / ORAL	652 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, FILM COATED / ORAL	1.68 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	CAPSULE, EXTENDED RELEASE / ORAL	0.26 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, COATED / ORAL	7.93 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	OINTMENT / TOPICAL	0.01 %w/w		Exact identifier — unii candidate 22 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SOLUTION / INTRAVENOUS	3.11 %w/v		Exact identifier — unii candidate 6 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	CAPSULE, EXTENDED RELEASE / ORAL		4 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SUPPOSITORY / RECTAL	375 mg		Exact identifier — unii candidate 6 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	ELIXIR / ORAL	0.15 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	INJECTION, SUSPENSION / SUBCUTANEOUS	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	CAPSULE, DELAYED RELEASE / ORAL	0.22 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	SOAP / TOPICAL	NA		Exact identifier — unii candidate 11 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	LIQUID / ORAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, DELAYED RELEASE / ORAL	0.1 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, EXTENDED RELEASE / ORAL	2.03 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, SUGAR COATED / ORAL	NA		Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SOLUTION / TOPICAL	0.06 %w/w		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SUSPENSION / ORAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	CAPSULE / ORAL		4 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	INJECTION / SUBCUTANEOUS	0.02 %w/v		Exact identifier — unii candidate 6 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	TABLET, COATED / ORAL	24.12 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	CAPSULE / ORAL		44 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET / ORAL	180 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, EXTENDED RELEASE / ORAL	0.01 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	TABLET, COATED / ORAL	213.7 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, CHEWABLE / ORAL	4.5 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, DELAYED RELEASE / ORAL		3 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	LOTION / TOPICAL	16 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET / SUBLINGUAL	0.11 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SOLUTION / ORAL	1 mg/1ml		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	TABLET / BUCCAL	0.01 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	OINTMENT / TOPICAL	20 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
YELLOW WAX	YELLOW WAX	2ZA36H0S2V	CAPSULE, EXTENDED RELEASE / ORAL	80.67 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SOLUTION / RESPIRATORY (INHALATION)	3.11 %w/v		Exact identifier — unii candidate 6 equally ranked IID candidates
FD&C BLUE NO. 2	FD&C BLUE NO. 2	L06K8R7DQK	TABLET, EXTENDED RELEASE / ORAL	2.78 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SYRUP / ORAL	0.1 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET / BUCCAL	0.11 mg		Exact identifier — unii candidate 22 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
07e06871-2141-46b7-84b2-dbd169c52128			d4adaa46-062e-4c1e-9d9c-e7073463a40d	2014-02-20	Warnings	Exact identifier spl id: 07e06871-2141-46b7-84b2-dbd169c52128 spl set id: d4adaa46-062e-4c1e-9d9c-e7073463a40d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.