SHYNOMORE LUBRICANT

Manufacturer
Bluette Co., Ltd. | Daeduck Lab. Co.,Ltd.
Effective date
2018-02-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:19

Label at a glance#

ProductSHYNOMORE LUBRICANT
Active ingredientCENTELLA ASIATICA
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Centella Asiatica Extract

INACTIVE INGREDIENT SECTION

Sodium Hyaluronate, Hamamelis Virginiana (Witch Hazel) Leaf Extract, etc.

OTC - PURPOSE SECTION

Water-soluble massage gel

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children

INDICATIONS & USAGE SECTION

With clean hands, dispense an appropriate amount and apply on skin, massaging gently

WARNINGS SECTION

Precautions for Use

If any of the following conditions occur, discontinue use immediately and consult a dermatologist. Continuous use will cause symptoms to worsen.

1) In case of skin reaction such as red spots, swelling, itch or irritation etc. during use

2) In case of the above skin reaction when applied area is exposed to direct sunlight

Do not use on damaged skin area such as wound, rash or skin infection

Storage and Handling

1) Close lid tightly after use

2) Keep out of reach of infants and children

3) Store in a cool, dry place away from direct sunlight

4) Avoid eye area

DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72072-0001-12020-01-31C16284748780-19d75b9d1-188a-f424-e053-dadaa90a57ce641fbbe5-dd60-31e2-e053-2991aa0af804

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72072-0001-1SHYNOMORE LUBRICANT100 mL in 1 TUBEGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72072-0001SHYNOMORE LUBRICANT (CENTELLA ASIATICA EXTRACT) GEL [BLUETTE CO., LTD.]1Legacy NDC, 1 package rows20180201_641fbbe5-dd60-31e2-e053-2991aa0af804.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72072-000172072-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
641fbbe5-dd67-31e2-e053-2991aa0af804641fbbe5-dd60-31e2-e053-2991aa0af8042018-02-01WarningsExact identifier
spl id: 641fbbe5-dd67-31e2-e053-2991aa0af804
spl set id: 641fbbe5-dd60-31e2-e053-2991aa0af804

Reported adverse events (FAERS/openFDA)#

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