FDA.reportPublic FDA data

TONG LUO QU TONG GAO

Manufacturer
HENAN LINGRUI PHARMACEUTICAL CO LTD
Effective date
2010-06-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:24:45

Label at a glance#

ProductTONG LUO QU TONG GAO
Active ingredientCAMPHOR (NATURAL), MENTHOL
Label structure12 sections

Storage and handling

Other information keep container tightly closed store below 20º C (68E F) in a dry area

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Camphor 5%
Menthol 3.4%

OTC - PURPOSE SECTION

Purposes

External Analgesic

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

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

OTC - DO NOT USE SECTION

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 hypersensitivities to this product
  • otherwise than as directed

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are

  • pregnant
  • taking other medications

OTC - WHEN USING SECTION

When using this product

  • avoid contact with the eyes or mucous membranes
  • do not bandage tightly
  • supervise use by children
  • use caution if prone to allergic reactions

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison
Control Center right away.

DOSAGE & ADMINISTRATION SECTION

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.

STORAGE AND HANDLING SECTION

Other information

  • keep container tightly closed
  • store below 20º C (68E F) in a dry area

INACTIVE INGREDIENT SECTION

Inactive ingredients Chinese rhubarb rhizome and root, cinnamon bark, clove,
dimethyl sulfoxide, dong-quai root, ginger rhizome, greater galangal rhizome, green
peppercorns, lanolin, long pepper (Piper longum L.) fruit, paraffin, petrolatum, rosin,
safflower flowers, Sichuan lovage rhizome, Sichuan pepper [Zanthoxylum piperitum (L.)
DC.] peel, and zinc oxide, on a rubberized fabric support with a paper backing.

OTC - QUESTIONS SECTION

Questions or comments? (888) 221-3496 M-F 9 am to 5 pm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TONG LUO QU TONG GAO PAIN RELIEVING POULTICE NDC 44217-100-01 4 PLASTERS EACH PLASTER 2.75 IN X 3.94 IN (7 CM X 10 CM)IMAGE OF BOXIMAGE OF BOX

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046583camphor 5 % / menthol 3.4 % Medicated PatchPSN3
1046583camphor 0.05 MG/MG / menthol 0.034 MG/MG Medicated PatchSCD3
1046583camphor 5 % / menthol 3.4 % Medicated PatchSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42217-100-012019-10-21C16284748780-1956f9ecf-c894-621f-e053-dbdaa90a74adDRUG LISTING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42217-100-01TONG LUO QU TONG GAO4 in 1 BOXPOULTICE43

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42217-100TONG LUO QU TONG GAO (CAMPHOR AND MENTHOL) POULTICE [HENAN LINGRUI PHARMACEUTICAL CO LTD]3Legacy NDC, 1 package rows20100609_8a7c4eab-363b-4faf-94e2-6d479fe18908.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9413
MENTHOLACTIVE INGREDIENTL7T10EIP3A3
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9413
MENTHOLACTIVE MOIETYL7T10EIP3A3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42217-10042217-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6df80051-a6eb-4d58-9670-496ec1c6bebd8a7c4eab-363b-4faf-94e2-6d479fe189082010-06-02Exact identifier
spl id: 6df80051-a6eb-4d58-9670-496ec1c6bebd
spl set id: 8a7c4eab-363b-4faf-94e2-6d479fe18908

Reported adverse events (FAERS/openFDA)#

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