WeTTrust Inclear

Manufacturer
WeTTrust Korea Co., Ltd | Cit Co., Ltd.
Effective date
2019-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:49:51

Label at a glance#

ProductWeTTrust Inclear
Active ingredientGlycerin
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Glycerin 6.50%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: water, hydroxyethylcellulose, lactic acid, sodium citrate, methylparaben, disodium EDTA, sodium hyaluronate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Cleansing vagina, maintaining vagina pH balanced, and improving odor and abnormal discharge (keep vagina fresh and clean)

WARNINGS

WARNINGS SECTION

Warnings: 1. Stop using the product and consult with your general practitioner for advice if any of the following signs or symptoms appear; rash, swelling, itching and irritation during its use 2. Do not use the product for any other purpose than vaginal cleaning. Do not use this product in eyes, nose, ears and anus. 3. In case of contacting with the cleansing gel in the eyes, immediately rinse with clean water. 4. This product is single-use disposable vaginal cleanser. Please do not reuse. 5. Consult with your general practitioner for advice if you wish to use this product during pregnancy. 6. This product does not provide contraception effects. Be aware that the contraception effects may decrease if you use this product after using spermicides like vaginal contraceptive film. 7. Do not use if the individual package or any part of the applicator has been broken or damaged.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: 1. Wash hands before opening the package. 2. Tear off the individual package. 3. Take out half of the applicator and hold the cap with fingers, then remove the cap by bending it downwards at 45 degrees. 4. Take out the applicator and get into a comfortable position. Then, insert the applicator approx. 5-8cm (from the tip). 5. Push the plunger to release cleansing gel. 6. Gently pull the applicator out of the vagina.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: 1.7g / recommended to use one at a time.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

Image of cartonImage of carton

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59543-5002-12022-10-18C16284748780-1ba0f9c33-164a-a910-e053-dadaa90a0b850479eaa9-0faa-467a-80de-5cd52ff291da
59543-5002-12021-01-29C16284748780-1ba0f9c33-164a-a910-e053-dadaa90a0b850479eaa9-0faa-467a-80de-5cd52ff291da

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
59543-500259543-5002-1

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
GlycerinPDC6A3C0OXACTIB
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
578c1ea0-6f0c-4daf-a4f0-71a2472a77b70479eaa9-0faa-467a-80de-5cd52ff291da2022-10-18WarningsExact identifier
spl set id: 0479eaa9-0faa-467a-80de-5cd52ff291da

Reported adverse events (FAERS/openFDA)#

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