WORMWOOD BALM

Manufacturer
Shenzhen Furuizhilian keji Co., Ltd.
Effective date
2024-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:15:17

Label at a glance#

ProductWORMWOOD BALM
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

MENTHOL 0.5%

OTC - PURPOSE SECTION

Insect Repellents

INDICATIONS & USAGE SECTION

Make sure the application area is clean and dry.
Apply to the mosquito bites, or to the limbs or other parts to prevent bites.

WARNINGS SECTION

For external use only
Don't eat, avoid contact with your eyes.

OTC - STOP USE SECTION

irritation and redness develop. If condition persists more than 48 hours.

OTC - WHEN USING SECTION

Do not get into eyes.
If contact occurs, rinse eyes thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INACTIVE INGREDIENT SECTION

Artemisia Argyi Leaf Extract, Peppermint Extract, Menthol, Beeswax

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84445-004-012025-07-29C16284748780-13b156c62-33ee-fb37-e063-e6dba90a4e07WORMWOOD BALM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84445-004-01WORMWOOD BALM30 g in 1 BOTTLECREAM301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84445-004WORMWOOD BALM (CHLORHEXIDINE DIACETATE) CREAM [SHENZHEN FURUIZHILIAN KEJI CO., LTD.]11 package rows20240716_1d456d38-824b-5ebe-e063-6294a90a082d.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
84445-00484445-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
1d456d38-824c-5ebe-e063-6294a90a082d1d456d38-824b-5ebe-e063-6294a90a082d2024-07-15WarningsExact identifier
spl id: 1d456d38-824c-5ebe-e063-6294a90a082d
spl set id: 1d456d38-824b-5ebe-e063-6294a90a082d

Reported adverse events (FAERS/openFDA)#

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