Yiyongxueweitie

Manufacturer
Beijing Shenzhou Pharmaceutical
Effective date
2020-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:20

Label at a glance#

ProductYiyongxueweitie
Active ingredientCAMPHOR (NATURAL)
Label structure14 sections

Indications and uses

Uses for the temporary relief of minor pain

Dosage and administration

■Adults and children 12 years of age and older: apply it to the painful area or acupoint as directed. If needed can use bandages to secure. Proper temperature can increase the effect. ■Use 1 to 2 plasters every 24 hours ■Apply the plaster to the affected area for 1 to 2 hours ■Children under 12 years of age: do not use or consult a doctor.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 1%.................……….…….External analgesic

OTC - ASK DOCTOR SECTION

Do not use otherwise than as directed

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning

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

If pregnant

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant, ask a health professional before use

Directions

DOSAGE & ADMINISTRATION SECTION

■Adults and children 12 years of age and older: apply it to the painful area or acupoint as directed. If needed can use bandages to secure. Proper temperature can increase the effect.
■Use 1 to 2 plasters every 24 hours
■Apply the plaster to the affected area for 1 to 2 hours
■Children under 12 years of age: do not use or consult a doctor.

Other information

OTHER SAFETY INFORMATION

■Store at room temperature, 10 ℃ to 30℃ (50℉ to 86℉)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Achyranthes bidentate, Aconitum carmichaeli, Angelica sinensis, Arisaema erubescens, Carthamus tinctorius, Cinnamomum cassia, Ligusticum chuanxiong, Notopterygium incisum, Paeonia lactiflora, Speranskia tuberculate, Zingiber officinale

Purpose

OTC - PURPOSE SECTION

External analgesic

Do not use

OTC - DO NOT USE SECTION

■on wounds

■irritated or damaged skin

■sensitive skin

When using this product

OTC - WHEN USING SECTION

■Avoid contact with the eyes
■Do not use more than 2 plasters a day in same area
■Do not use 1 hour 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
■Redness is present

Use

WARNINGS SECTION

For external use only

Uses

INDICATIONS & USAGE SECTION

Uses for the temporary relief of minor pain

Inner Bag

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Inner Bag

Inner BagInner Bag

External Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

External Box

External BoxExternal Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1725038camphor 1 % Medicated PatchPSN1
1725038camphor 0.01 MG/MG Medicated PatchSCD1
1725038camphor 1 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77547-001-012022-01-28C16284748780-1d6a99b39-c2e2-a426-e053-dadaa90af4c2Yiyongxueweitie

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77547-001-01Yiyongxueweitie2 in 1 PACKAGEPLASTER21
77547-001-01Yiyongxueweitie24 in 1 BOXPLASTER241
77547-001-02Yiyongxueweitie1 g in 1 PACKAGEPLASTER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77547-001YIYONGXUEWEITIE (CAMPHOR) PLASTER [BEIJING SHENZHOU PHARMACEUTICAL]1Legacy NDC, 3 package rows20200619_af3f789e-bbd0-44ac-8377-14aa4b0b4a2b.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77547-00177547-001-02, 77547-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
a8617e8e-2234-f700-e053-2995a90a7499af3f789e-bbd0-44ac-8377-14aa4b0b4a2b2020-06-18WarningsExact identifier
spl id: a8617e8e-2234-f700-e053-2995a90a7499
spl set id: af3f789e-bbd0-44ac-8377-14aa4b0b4a2b

Reported adverse events (FAERS/openFDA)#

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