LADY GOONG

Manufacturer
Lady House Co., Ltd.
Effective date
2020-10-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:14

Label at a glance#

ProductLADY GOONG
Active ingredientETHYLHEXYLGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ethylhexylglycerin

OTC - PURPOSE SECTION

moisturizing cleaning shrink maintaining pH balance

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

apply proper amount to the vaginal

WARNINGS SECTION

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for vaginal use only

INACTIVE INGREDIENT SECTION

water, sorbitol, etc

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80766-0005-12022-01-28C16284748780-1d6a99b39-b2a9-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80766-0005-1LADY GOONG1.6 g in 1 APPLICATORLIQUID1.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80766-0005LADY GOONG (ETHYLHEXYLGLYCERIN) LIQUID [LADY HOUSE CO., LTD.]1Legacy NDC, 1 package rows20201022_b23944f7-f8c0-b2a4-e053-2a95a90a1b87.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80766-000580766-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYLGLYCERIN147D247K3PACTIB
WATER059QF0KO0RIACT

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
b23944f7-f8bf-b2a4-e053-2a95a90a1b87b23944f7-f8c0-b2a4-e053-2a95a90a1b872020-10-21WarningsExact identifier
spl id: b23944f7-f8bf-b2a4-e053-2a95a90a1b87
spl set id: b23944f7-f8c0-b2a4-e053-2a95a90a1b87

Reported adverse events (FAERS/openFDA)#

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