FDA.reportPublic FDA data

ZANG QI

Manufacturer
QINGHAI ZANGYUANTANG BIO-TECH CO LTD
Effective date
2010-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:44

Label at a glance#

ProductZANG QI
Active ingredientCAMPHOR (NATURAL)
Label structure11 sections

Storage and handling

Other information keep tightly sealed, protected from light store at room temperature away from heat

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Camphor 3.1%

OTC - PURPOSE SECTION

Purpose

Topical analgesic

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

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

OTC - DO NOT USE SECTION

Do not use

  • on wounds
  • on irritated or damaged skin

OTC - WHEN USING SECTION

When using this product

  • avoid contact with the eyes and mucous membranes
  • do not bandage tightly or cover with any kind of wrap except loose clothing

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
  • nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs
  • when using for pain of arthritis:
    • if pain persists for more than 10 days
    • if 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:
    • clean and dry the affected area
    • remove the protective film from the plaster
    • carefully tear open a corner of the foil packet using the notch located on the seal about 1/4 inch from one end
    • squeeze the entire contents of the foil packet evenly into the center of the pad
    • apply the plaster to the affected area
    • keep the plaster on the affected area for 8-12 hours
    • use 1 or 2 plasters on the affected area daily, as need, but never more than 3 or 4
  • children under 12 years of age: do not use, consult a doctor

STORAGE AND HANDLING SECTION

Other information

  • keep tightly sealed, protected from light
  • store at room temperature away from heat

INACTIVE INGREDIENT SECTION

Inactive ingredients acidic acid, 60% alcohol, bamboo charcoal,
maifanshi stone powder, pepper leaves, and poplar leaves on an elastic, skin
colored, cotton fabric with acrylic acid resin, covered with a protective film.

OTC - QUESTIONS SECTION

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

  • you may also use this number to report serious adverse events associated with the use of this product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZANG QI PAIN RELIEVING PLASTER NDC 51673-001-01 5 PLASTERS EACH PLASTER 4.75 IN X 3.5 IN (12 CM X 9 CM)IMAGE OF CARTONIMAGE OF CARTON

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046544camphor 3.1 % Medicated PatchPSN1
1046544camphor 0.031 MG/MG Medicated PatchSCD1
1046544camphor 3.1 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51673-001-012019-10-21C16284748780-1956f9ecf-bb98-621f-e053-dbdaa90a74adDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51673-001-01ZANG QI5 in 1 BOXPLASTER51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51673-001ZANG QI (CAMPHOR (NATURAL)) PLASTER [QINGHAI ZANGYUANTANG BIO-TECH CO LTD]1Legacy NDC, 1 package rows20100609_0fbb7035-0f36-46d2-bf7a-b13e4051e9ec.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9411
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9411

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51673-00151673-001-01

Ingredients#

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

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

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

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
93eef5c7-3b70-4633-b4ed-c5ba1aafe2280fbb7035-0f36-46d2-bf7a-b13e4051e9ec2010-06-04Exact identifier
spl id: 93eef5c7-3b70-4633-b4ed-c5ba1aafe228
spl set id: 0fbb7035-0f36-46d2-bf7a-b13e4051e9ec

Reported adverse events (FAERS/openFDA)#

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