TONG LUO QU TONG GAO

Manufacturer: Henan Lingrui Pharmaceutical Co.; Ltd
Effective date: 2014-03-01
Label type: HUMAN OTC DRUG LABEL
Version: 3029
Source: full-release
Hydrated at: 2026-05-31 22:38:34

Label at a glance#

ProductTONG LUO QU TONG GAO

Active ingredientCAMPHOR (NATURAL), MENTHOL

Label structure13 sections

Indications and uses

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

Dosage and administration

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.

Storage and handling

Keep container tightly closed. Store below 20 degree centigrade (68 E F) in a dry area.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Camphor 5%

Menthol 3.4%

PURPOSE

OTC - PURPOSE SECTION

Camphor External Analgesic

Menthol External Analgesic

USES

INDICATIONS & USAGE SECTION

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

simple backache

arthritis

strains

bruises

sprains

DO NOT USE

WARNINGS SECTION

on wounds

on irritated or damaged skin

if the appearance of this product has changed

in excess of 12 hours

if you have known hypersensitives to this product

otherwise than as directed

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

OTC - ASK DOCTOR/PHARMACIST SECTION

pregnant

taking other medications

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

avoid contact with the eye or mucous membrances

do not bandage tightly

supervise use by children

use caution if prone to allergic reactions

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 irritaion of the skin develops

when using for pain of athritis

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Keep container tightly closed.

Store below 20 degree centigrade (68 E F) in a dry area.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

CHINESE RHUBARB ROOT, CINNAMOMUM AROMATICUM WHOLE, CLOVE, ANGELICA SINENSIS ROOT, GINGER, GREEN PEPPERCORN, LONG PEPPER, BORNEOL, NATURAL LATEX RUBBER, ROSIN, SAFFLOWER, LIGUSTICUM WALLICHII ROOT, ZANTHOXYLUM PIPERITUM WHOLE, PETROLATUM, ZINC OXIDE, LANOLIN, PARAFFIN, DIMETHYL SULFOXIDE

Questions or Comments?

OTC - QUESTIONS SECTION

E-mail: info@bjwellspring.com

DRUG FACTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046583	camphor 5 % / menthol 3.4 % Medicated Patch	PSN	3029
1046583	camphor 0.05 MG/MG / menthol 0.034 MG/MG Medicated Patch	SCD	3029
1046583	camphor 5 % / menthol 3.4 % Medicated Patch	SY	3029

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
42217-200-05	2019-11-27	C162847	48780-1	9855e2a2-32eb-60a7-e053-dbdaa90a05bd	Henan Lingrui Pharmaceutical Co.; Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
42217-200-05	TONG LUO QU TONG GAO	1 g in 1 PATCH	PLASTER	1		3029
42217-200-05	TONG LUO QU TONG GAO	5 in 1 BOX	PLASTER	5		3029

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42217-200	TONG LUO QU TONG GAO (CAMPHOR, MENTHOL) PLASTER [HENAN LINGRUI PHARMACEUTICAL CO.; LTD]	3029	Legacy NDC, 2 package rows	20140303_821e40a3-1c10-4069-bbbb-920fa9d35dab.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
CAMPHOR (NATURAL)	ACTIVE INGREDIENT	N20HL7Q941	3029
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	3029
CAMPHOR (NATURAL)	ACTIVE MOIETY	N20HL7Q941	3029
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	3029
ANGELICA SINENSIS ROOT	INACTIVE INGREDIENT	B66F4574UG	3029
BORNEOL	INACTIVE INGREDIENT	M89NIB437X	3029
CHINESE RHUBARB ROOT	INACTIVE INGREDIENT	5U759027OH	3029
CINNAMOMUM AROMATICUM WHOLE	INACTIVE INGREDIENT	9BPF21T8ZR	3029
CLOVE	INACTIVE INGREDIENT	K48IKT5321	3029
DIMETHYL SULFOXIDE	INACTIVE INGREDIENT	YOW8V9698H	3029
GINGER	INACTIVE INGREDIENT	C5529G5JPQ	3029
GREEN PEPPERCORN	INACTIVE INGREDIENT	6G53L8ESRK	3029
LANOLIN	INACTIVE INGREDIENT	7EV65EAW6H	3029
LIGUSTICUM WALLICHII ROOT	INACTIVE INGREDIENT	R81AD159QS	3029
LONG PEPPER	INACTIVE INGREDIENT	2NMG4EA7B1	3029
NATURAL LATEX RUBBER	INACTIVE INGREDIENT	2LQ0UUW8IN	3029
PARAFFIN	INACTIVE INGREDIENT	I9O0E3H2ZE	3029
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	3029
ROSIN	INACTIVE INGREDIENT	88S87KL877	3029
SAFFLOWER	INACTIVE INGREDIENT	4VBL71TY4Y	3029
ZANTHOXYLUM PIPERITUM WHOLE	INACTIVE INGREDIENT	Y8IKP41338	3029
ZINC OXIDE	INACTIVE INGREDIENT	SOI2LOH54Z	3029

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

TONG LUO QU TONG GAO
CAMPHOR, MENTHOL
CAMPHOR (NATURAL)
MENTHOL
CHINESE RHUBARB ROOT
CINNAMOMUM AROMATICUM WHOLE
CLOVE
ANGELICA SINENSIS ROOT
GINGER
GREEN PEPPERCORN
LONG PEPPER
BORNEOL
NATURAL LATEX RUBBER
ROSIN
SAFFLOWER
LIGUSTICUM WALLICHII ROOT
ZANTHOXYLUM PIPERITUM WHOLE
PETROLATUM
ZINC OXIDE
LANOLIN
PARAFFIN
DIMETHYL SULFOXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
42217-200	42217-200-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CAMPHOR (NATURAL)	N20HL7Q941	ACTIB
MENTHOL	L7T10EIP3A	ACTIB
CHINESE RHUBARB ROOT	5U759027OH	IACT
CINNAMOMUM AROMATICUM WHOLE	9BPF21T8ZR	IACT
CLOVE	K48IKT5321	IACT
ANGELICA SINENSIS ROOT	B66F4574UG	IACT
GINGER	C5529G5JPQ	IACT
GREEN PEPPERCORN	6G53L8ESRK	IACT
LONG PEPPER	2NMG4EA7B1	IACT
BORNEOL	M89NIB437X	IACT
NATURAL LATEX RUBBER	2LQ0UUW8IN	IACT
ROSIN	88S87KL877	IACT
SAFFLOWER	4VBL71TY4Y	IACT
LIGUSTICUM WALLICHII ROOT	R81AD159QS	IACT
ZANTHOXYLUM PIPERITUM WHOLE	Y8IKP41338	IACT
PETROLATUM	4T6H12BN9U	IACT
ZINC OXIDE	SOI2LOH54Z	IACT
LANOLIN	7EV65EAW6H	IACT
PARAFFIN	I9O0E3H2ZE	IACT
DIMETHYL SULFOXIDE	YOW8V9698H	IACT

Source Document#

Source XML · Source PDF

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 · 53 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
LANOLIN	LANOLIN	7EV65EAW6H	SHAMPOO / TOPICAL	2 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	CREAM / TOPICAL		300 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	OINTMENT / RECTAL		105 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	SOAP / TOPICAL	0.4 %w/w		Exact identifier — unii candidate 11 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	OINTMENT / RECTAL		38 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	OINTMENT / TOPICAL		2860 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SPONGE / TOPICAL	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	AEROSOL, FOAM / TOPICAL	7.9 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SUPPOSITORY / VAGINAL	27 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / TOPICAL		7275 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	OINTMENT / TOPICAL	10 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / VAGINAL		4084 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / AURICULAR (OTIC)	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
DIMETHYL SULFOXIDE	DIMETHYL SULFOXIDE	YOW8V9698H	IMPLANT / SUBCUTANEOUS	104 mg		Exact identifier — unii candidate 4 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT, AUGMENTED / TOPICAL	81.94 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CREAM, AUGMENTED / TOPICAL	26 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
ROSIN	ROSIN	88S87KL877	CAPSULE / ORAL	NA		Exact identifier — unii candidate 3 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	OINTMENT / OPHTHALMIC	3 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / OPHTHALMIC	88.4 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CAPSULE, EXTENDED RELEASE / ORAL	0.07 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
ROSIN	ROSIN	88S87KL877	TABLET, EXTENDED RELEASE / ORAL	8.99 mg		Exact identifier — unii candidate 3 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	TABLET, EXTENDED RELEASE / ORAL	0.18 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET / ORAL	0.7 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
PETROLATUM	PETROLATUM	4T6H12BN9U	CAPSULE / VAGINAL	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	CAPSULE, EXTENDED RELEASE / ORAL		100 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	SUSPENSION / TOPICAL		11726 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
DIMETHYL SULFOXIDE	DIMETHYL SULFOXIDE	YOW8V9698H	SOLUTION / TOPICAL		8008 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
DIMETHYL SULFOXIDE	DIMETHYL SULFOXIDE	YOW8V9698H	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS	NA		Exact identifier — unii candidate 4 equally ranked IID candidates
ROSIN	ROSIN	88S87KL877	TABLET, COATED / ORAL	10 mg		Exact identifier — unii candidate 3 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SOLUTION / INTRAVENOUS	3.11 %w/v		Exact identifier — unii candidate 6 equally ranked IID candidates
GINGER	GINGER	C5529G5JPQ	ELIXIR / ORAL	10 mg/5ml		Exact identifier — unii candidate 2 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
GINGER	GINGER	C5529G5JPQ	SYRUP / ORAL	0.05 ml/5ml		Exact identifier — unii candidate 2 equally ranked IID candidates
DIMETHYL SULFOXIDE	DIMETHYL SULFOXIDE	YOW8V9698H	LOTION / TOPICAL	45.5 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	EMULSION / TOPICAL	7.8 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET, EXTENDED RELEASE / ORAL		321 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	AEROSOL, FOAM / TOPICAL		14235 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SOAP / TOPICAL	0.85 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	LOTION / TOPICAL	25 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	LIQUID / RESPIRATORY (INHALATION)	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CREAM / TOPICAL		4213 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	EMULSION / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	LOTION / TOPICAL	1.5 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SUPPOSITORY / RECTAL	375 mg		Exact identifier — unii candidate 6 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET, DELAYED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	LOTION / TOPICAL	16 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	CREAM / VAGINAL	2 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	CREAM / TOPICAL		10 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	INJECTION, SUSPENSION / SUBCUTANEOUS	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	TABLET / ORAL	3.5 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
LANOLIN	LANOLIN	7EV65EAW6H	SPRAY / NASAL	NA		Exact identifier — unii candidate 9 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET, COATED / ORAL	0.07 mg		Exact identifier — unii candidate 11 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
823a4603-d2cd-416c-86c4-d50c3f53a439			821e40a3-1c10-4069-bbbb-920fa9d35dab	2014-03-01	Warnings	Exact identifier spl id: 823a4603-d2cd-416c-86c4-d50c3f53a439 spl set id: 821e40a3-1c10-4069-bbbb-920fa9d35dab

Reported adverse events (FAERS/openFDA)#

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