Heibaitong Pain Relieving Patch

Manufacturer
Harbin Kangyou Pharmaceutical Limited Company
Effective date
2018-12-11
Label type
HUMAN OTC DRUG LABEL
Version
32467
Source
full-release
Hydrated at
2026-05-31 22:57:35

Label at a glance#

ProductHeibaitong Pain Relieving Patch
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure15 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: This product can be applied up to 168 hours of repeated uses. Remove the package from package. Heat up the patch until it easily gets separated and it becomes soft and glossy (avoid touching on skin when it is hot from the heat). Apply one or two patches to affected area once a day. Remove after every 6-12 hours depending on symptoms. During treatments, it is normal t...

Storage and handling

Keep container tightly closed. Store below 20 ℃ (68 ℉) in a dry area.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Menthol       5%

Camphor     3.5%

PURPOSE

OTC - PURPOSE SECTION

Menthol         External Analgesic

Camphor       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.

Warnings

WARNINGS SECTION

For External Use only.

Do not use

OTC - DO NOT USE SECTION

on wounds.
on irritated or damaged skin.
if the appearance of this product has changed.
in excess of 12 hours.
if you are hypersensitive 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 membranes.
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 irritation of the skin develops.
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: This product can be applied up to 168 hours of repeated uses. Remove the package from package. Heat up the patch until it easily gets separated and it becomes soft and glossy (avoid touching on skin when it is hot from the heat). Apply one or two patches to affected area once a day. Remove after every 6-12 hours depending on symptoms. During treatments, it is normal to feel the heat from patch itself. It can be removed anytime if discomfort occurs. 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 ℃ (68 ℉) in a dry area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

NOTOPTERYGIUM INCISUM ROOT, ANGELICA PUBESCENS ROOT, SINOMENIUM ACUTUM STEM, PERIPLOCA SEPIUM ROOT BARK, SAPOSHNIKOVIA DIVARICATA ROOT, ATRACTYLODES LANCEA ROOT, CNIDIUM MONNIERI FRUIT, ALPINIA OFFICINARUM WHOLE, CUMINUM CYMINUM WHOLE, CINNAMON, ANGELICA SINENSIS ROOT, PAEONIA LACTIFLORA ROOT, PAPAYA, CAESALPINIA SAPPAN WOOD, RHUBARB, PINUS TABULIFORMIS BARK, DIPSACUS CHINENSIS WHOLE, LIGUSTICUM WALLICHII ROOT, ANGELICA DAHURICA ROOT, FRANKINCENSE OIL, MYRRH, BORNEOL, CLOVE OIL, CHINESE CINNAMON, CINNAMOMUM CASSIA TWIG, PANAX NOTOGINSENG ROOT, SAFFRON, ERYCIBE OBTUSIFOLIA STEM, PIPER KADSURA STEM, FOSSILIZED MAMMAL BONE

Questions or Comments?

OTC - QUESTIONS SECTION

Relief Saturated LLC
Alhambra, California 91801

Call (626) 247-0304 or
E-mail: kyle.hsieh18@gmail.com

Manufactured by Kangyou Pharmaceutical Limited Company2nd Building, 1st Floor, 8 Km Half of Ha Double Highway in Dao Li DistrictHarbin 150076, China

SPL UNCLASSIFIED SECTION

Distributed by

Relief Saturated LLC
Alhambra, California 91801 USA

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2055287camphor 3.5 % / menthol 5 % Medicated PatchPSN32467
2055287camphor 0.035 MG/MG / menthol 0.05 MG/MG Medicated PatchSCD32467
2055287camphor 3.5 % / menthol 5 % Medicated PatchSY32467

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72328-001-012020-01-31C16284748780-19d75b9cf-e8d6-f424-e053-dadaa90a57ceHarbin Kangyou Pharmaceutical Limited Company

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72328-001-01Heibaitong Pain Relieving Patch13 g in 1 PATCHPATCH1332467
72328-001-01Heibaitong Pain Relieving Patch1 in 1 POUCHPATCH132467

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72328-001HEIBAITONG PAIN RELIEVING PATCH (MENTHOL, CAMPHOR) PATCH [HARBIN KANGYOU PHARMACEUTICAL LIMITED COMPANY]32467Legacy NDC, 2 package rows20181212_f13500bd-9357-42df-84fa-bf9924f9523e.zip

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72328-00172328-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

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
28a53b6f-d9a8-435b-bde0-c42fe088ef36f13500bd-9357-42df-84fa-bf9924f9523e2018-12-11WarningsExact identifier
spl id: 28a53b6f-d9a8-435b-bde0-c42fe088ef36
spl set id: f13500bd-9357-42df-84fa-bf9924f9523e

Reported adverse events (FAERS/openFDA)#

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