FDA.reportPublic FDA data

WeDol Water-based personal lubricant

Manufacturer
Shenzhenshi Huaxiang Technology Co.,Ltd.
Effective date
2019-08-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:25

Label at a glance#

ProductWeDol Water-based personal lubricant
Active ingredientHYDROXYETHYL CELLULOSE (140 CPS AT 5%)
Label structure12 sections

Label contents#

Full prescribing information#

active ingredient

OTC - ACTIVE INGREDIENT SECTION

active ingredientactive ingredient

indication usage

INDICATIONS & USAGE SECTION

instructioninstruction

instructions for use

INSTRUCTIONS FOR USE SECTION

instruction for useinstruction for use

inactive

INACTIVE INGREDIENT SECTION

inactiveinactive

ask a doctor

OTC - ASK DOCTOR SECTION

ask a doctorask a doctor

warnings

WARNINGS SECTION

warningwarning

stop using

OTC - STOP USE SECTION

stop usestop use

when using

OTC - WHEN USING SECTION

when usingwhen using

keep out of

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of childrenkeep out of children

dosage

DOSAGE & ADMINISTRATION SECTION

dosagedosage

purpose

OTC - PURPOSE SECTION

purposepurpose

package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73298-190-342021-01-29C16284748780-1ba0f9c33-4710-a910-e053-dadaa90a0b859037ca36-5406-63f0-e053-2995a90a86cb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73298-190-33WeDol Water-based personal lubricant240 mL in 1 TUBEOIL2401
73298-190-34WeDol Water-based personal lubricant1 in 1 BOXOIL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73298-190WEDOL WATER-BASED PERSONAL LUBRICANT (WATER-BASED PERSONAL LUBRICANT) OIL [SHENZHENSHI HUAXIANG TECHNOLOGY CO.,LTD.]1Legacy NDC, 2 package rows20190915_9037ca36-5406-63f0-e053-2995a90a86cb.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73298-19073298-190-33, 73298-190-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYETHYL CELLULOSE (140 CPS AT 5%)8136Y38GY5ACTIB
PEG-7 DISTEARATEVU1ZWG290CIACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CHLORPHENESINI670DAL4SZIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

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
9037ca36-5407-63f0-e053-2995a90a86cb9037ca36-5406-63f0-e053-2995a90a86cb2019-08-16WarningsExact identifier
spl id: 9037ca36-5407-63f0-e053-2995a90a86cb
spl set id: 9037ca36-5406-63f0-e053-2995a90a86cb

Reported adverse events (FAERS/openFDA)#

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