FDA.reportPublic FDA data

KENX WATER BASED PERSONAL LUBRICANT

Manufacturer
SB Innovations LLC
Effective date
2025-02-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:55:52

Label at a glance#

ProductKENX WATER BASED PERSONAL LUBRICANT
Active ingredientHYDROXYETHYLCELLULOSE
Label structure10 sections

Storage and handling

Seal the product and avoid light. Store in a cool and dry place. Product shelf life: 3 years Please check on the print code.

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Apply and massage desired areas for a bilssful massage experience. Splash a bit on and enjoy!

WARNINGS SECTION

If iritation or discomfort occurs, discontinue use and consult a physician.

Very slippery on surfaces.

Clean spills immediately.

Keep out of reach of children and pets.

This product is not a contraceptive or spermicide.

WARNINGS AND PRECAUTIONS SECTION

Caution: For external use only. Avoid contact with eyes. please keep it out of rach of children.

STORAGE AND HANDLING SECTION

Seal the product and avoid light. Store in a cool and dry place.

Product shelf life: 3 years

Please check on the print code.

DOSAGE & ADMINISTRATION SECTION

6.7 FL.OZ (200ML)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

OTC - PURPOSE SECTION

Gently squeeze out an appropriate amount of lubricant, and evenly apply it on the desired area.

OTC - ACTIVE INGREDIENT SECTION

HYDROXYETHYL CELLULOSE

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylence Glycol, Saururus Chinensis Leaf/Root Extract, Taraxacum Officinale (Dandelion) Leaf Extract, Hydroxyethylcellulose, Hydroxyacetophenone, 1,2-Hexanediol, Carbomer, Triethanolamine, Stephania Tetrandra Extract, PEG-40 Hydrogenated Castor Oil, Disodum Edta, Parfum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product labelProduct label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85280-800-01KENX WATER BASED PERSONAL LUBRICANT30 mL in 1 BOTTLEOIL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85280-800KENX WATER BASED PERSONAL LUBRICANT (WATER BASED PERSONAL LUBRICANT) OIL [SB INNOVATIONS LLC]11 package rows20250226_2eaa7245-82b4-7d9c-e063-6394a90ab2f7.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85280-80085280-800-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
SAURURUS CHINENSIS WHOLE6DRV3D37XSIACT
HYDROXYETHYLCELLULOSET4V6TWG28DACTIB
2'-HYDROXYACETOPHENONE3E533Z76W0IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
TRIETHANOLAMINE9O3K93S3TKIACT
PARFUMIDINEA2Q2LHC6MAIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL 1,2-DISTEARATET65PN3O37HIACT
STEPHANIA TETRANDRA WHOLE7S7TV2F4XCIACT
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
WATER059QF0KO0RIACT
TARAXACUM OFFICINALE (DANDELION) ROOT9DE5YCO0RUIACT
CARBOMER0A5MM307FCIACT

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
2eaa7245-82b5-7d9c-e063-6394a90ab2f72eaa7245-82b4-7d9c-e063-6394a90ab2f72025-02-21WarningsExact identifier
spl id: 2eaa7245-82b5-7d9c-e063-6394a90ab2f7
spl set id: 2eaa7245-82b4-7d9c-e063-6394a90ab2f7

Reported adverse events (FAERS/openFDA)#

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