KAEWOON

Manufacturer
RNCARE
Effective date
2021-10-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:42:36

Label at a glance#

ProductKAEWOON
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.1%

OTC - PURPOSE SECTION

Hair Care

INDICATIONS & USAGE SECTION

Damaged hair care

DOSAGE & ADMINISTRATION SECTION

1. After wetting hairs and scalp with lukewarm water, lather hairs thoroughly with an appropriate amount of premium Kaewoon Shampoo.

2. Massage hair to removed all the dirt and waste and then, rinse.

3. For heavily damaged hair, you can use Premium Kaewoon Shampoo two times in a row to see a better result.

WARNINGS SECTION

In case of eye contact, immediately rinse with water

Stop use if unusual redness, swelling, soreness or irritation occur

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71237-002-022023-01-30C16284748780-1ba0f9c33-21cb-a910-e053-dadaa90a0b8571237-002_V3
71237-002-022021-10-04C16284748780-1ba0f9c33-21cb-a910-e053-dadaa90a0b8571237-002_V3
71237-002-022021-01-29C16284748780-1ba0f9c33-21cb-a910-e053-dadaa90a0b8571237-002_V3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71237-002-01KAEWOON500 mL in 1 BOTTLESHAMPOO5004
71237-002-02KAEWOON1 in 1 CARTONSHAMPOO14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71237-002KAEWOON (MENTHOL) SHAMPOO [RNCARE]4Legacy NDC, 2 package rows20211005_00c0d377-c7de-4617-b32f-4aac6da34b6e.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
71237-00271237-002-01, 71237-002-02

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
cd8af91d-0b46-b3e5-e053-2995a90a638e00c0d377-c7de-4617-b32f-4aac6da34b6e2021-10-04WarningsExact identifier
spl id: cd8af91d-0b46-b3e5-e053-2995a90a638e
spl set id: 00c0d377-c7de-4617-b32f-4aac6da34b6e

Reported adverse events (FAERS/openFDA)#

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