Jikimi Patch

Manufacturer
BM Pharmaceutical Co., Ltd.
Effective date
2020-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:50

Label at a glance#

ProductJikimi Patch
Active ingredientLEVOMENTHOL, ALCOHOL, EUCALYPTUS OIL
Label structure12 sections

Dosage and administration

Remove patch from film. Apply to affected area as topical aromatic diffusion not more than 3 to 4 times daily. Remove patch at most 24-36 hours application.

Storage and handling

Store at room temperature between 1-30oC (33.8-86oF). Avoid storing product in direct sunlight. Protect product from excessive moisture.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 7% w/w………………………...………. Antimicrobial

Levomenthol 3% w/w………………………...………. Antifungal

Eucalyptus oil 20% w/w…………………………...…. Antimicrobial

Purpose

OTC - PURPOSE SECTION

To help reduce bacteria.

Use

INDICATIONS & USAGE SECTION

Apply to affected area as topical aromatic diffusion.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • Do not use if you are allergic to any ingredients of this product.
  • Do not use in children under 6 and pregnant or breast-feeding.

OTC - WHEN USING SECTION

When using this product use only as directed. Use within 2 days after removing the film. Avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts. It happen headache. Conditions worsen.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Remove patch from film.
Apply to affected area as topical aromatic diffusion not more than 3 to 4 times daily.

Remove patch at most 24-36 hours application.

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature between 1-30oC (33.8-86oF).
  • Avoid storing product in direct sunlight.
  • Protect product from excessive moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Extract of fenugreek, Patchouli oil, Thyme oil.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Jikimi Ptach 4 pieceJikimi Ptach 4 piece

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76614-100-102022-01-28C16284748780-1d6a99b39-8bb1-a426-e053-dadaa90af4c2a4ed6dfb-e21b-9f32-e053-2a95a90ab001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76614-100-10Jikimi Patch4 in 1 PACKAGEPATCH41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76614-100JIKIMI PATCH (ANTI-BACTERIAL PATCH) PATCH [BM PHARMACEUTICAL CO., LTD.]1Legacy NDC, 1 package rows20200506_a4ed6dfb-e21b-9f32-e053-2a95a90ab001.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76614-10076614-100-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
a4eddb6d-0201-1b2e-e053-2a95a90a221da4ed6dfb-e21b-9f32-e053-2a95a90ab0012020-05-05WarningsExact identifier
spl id: a4eddb6d-0201-1b2e-e053-2a95a90a221d
spl set id: a4ed6dfb-e21b-9f32-e053-2a95a90ab001

Reported adverse events (FAERS/openFDA)#

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