FDA.reportPublic FDA data

UTIMI Water Based Personal Lubricant

Manufacturer
Shenzhen ZhiHuiChuangXiang Technology Co., Ltd
Effective date
2019-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:58:59

Label at a glance#

ProductUTIMI Water Based Personal Lubricant
Active ingredientHYDROXYETHYL CELLULOSE (140 CPS AT 5%)
Label structure16 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydroxyethyl Cellulose

Inactive ingredient

INACTIVE INGREDIENT SECTION

De-lonized Water
Glycerin
Propylene Glycol
Sodium Benzoate
Polysorbate 20
Disodium EDTA
Lactic Acid

Purpose

OTC - PURPOSE SECTION

Utimi Personal Lubricant is a water-based lubricant for penile or vaginal application, intended to moisturize and enhance the ease and comfort of intimate sexual activity as well as supplement for the body's natural lubrication.

This product is compatible with natural rubber latex, polyurethane and polyisoprene condoms.

When using

OTC - WHEN USING SECTION

Virginal / Anal dryness and/or intimate sexual activity.

This product is not a contraceptive and does not contain a spermicide.

Do not use

OTC - DO NOT USE SECTION

Do not use when wound or skin infection.

It should be cautiously used if you are kind of allergic constitution or you have inflammation.
Do not use if quality seal on the opening of the container is broken or missing.
Do not use if tamper-evident seal is removed or broken.

Stop use

OTC - STOP USE SECTION

If irritation or discomfort occurs, discontinue the use and consult a physician.
Very slippery on surfaces, clean spills immediately.

Ask doctor

OTC - ASK DOCTOR SECTION

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

Ask doctor/pharmacist

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask doctor/pharmacist when you current use other drugs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and away from eyes and ears.

Questions

OTC - QUESTIONS SECTION

Please contact us when you have any questions.

Pregnancy or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Pregnant or breast feeding women shall follow doctor advice.

Indications & usage

INDICATIONS & USAGE SECTION

This is a water-based lubricant for penile or vaginal application, intended to moisturize and enhance the ease and comfort of intimate sexual activity as well as supplement for the body's natural lubrication.

Apply a small amount to genital areas. Reapply as needed or desired.

Dosage & administration

DOSAGE & ADMINISTRATION SECTION

Apply a small amount to genital areas. Reapply as needed or desired.

Dosage forms & strengths

DOSAGE FORMS & STRENGTHS SECTION

The lubricant is like oil form.

One capsule (0.9g lubricant and 0.3g gelatin coated) once time.

The active ingredient strength is 0.324g.

Warnings

WARNINGS SECTION

If irritation or discomfort occurs, pleas discontinue to use and consult a physician.

Very slippery surfaces, clean the spills immediately.

This product is not a contraceptive or spermicide.

Keep out of children and pets' reach.

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

As attached.

Container Label_UtimiContainer Label_Utimi

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.utimi.com/Container Label_Utimi.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73000-225-202022-01-28C16284748780-1d6a99b39-846e-a426-e053-dadaa90af4c2Water Based Personal Lubricant, UTIMI, 30mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73000-225-20UTIMI Water Based Personal Lubricant30 mL in 1 BOTTLELOTION301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73000-225UTIMI WATER BASED PERSONAL LUBRICANT (PERSONAL LUBRICANT) LOTION [SHENZHEN ZHIHUICHUANGXIANG TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20190327_84d1b350-df6d-8c0c-e053-2a91aa0ad73f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73000-22573000-225-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
SODIUM BENZOATEOJ245FE5EUIACT
WATER059QF0KO0RIACT
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
HYDROXYETHYL CELLULOSE (140 CPS AT 5%)8136Y38GY5ACTIB
LACTIC ACID, DL-3B8D35Y7S4IACT

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
84d1b350-df53-8c0c-e053-2a91aa0ad73f84d1b350-df6d-8c0c-e053-2a91aa0ad73f2019-03-27WarningsExact identifier
spl id: 84d1b350-df53-8c0c-e053-2a91aa0ad73f
spl set id: 84d1b350-df6d-8c0c-e053-2a91aa0ad73f

Reported adverse events (FAERS/openFDA)#

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