FDA.reportPublic FDA data

UTIMI water based personal lubricant

Manufacturer
Shenzhen Guangdian Technology Co., Ltd
Effective date
2022-03-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:17:12

Label at a glance#

ProductUTIMI water based personal lubricant
Active ingredientHYDROXYETHYL CELLULOSE (140 CPS AT 5%)
Label structure13 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydroxyethyl Cellulose 1.27% w/w

Inactive ingredient

INACTIVE INGREDIENT SECTION

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

Indication for use

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.

Do not use

OTC - DO NOT USE SECTION

This product is not a contraceptive or spermicide.

Stop use

OTC - STOP USE SECTION

If irriation or discomfor occurs, please discontinue to use and consult a physician.

Very slippery surfaces, clean the spills immediately.

Ask doctor/physician

OTC - ASK DOCTOR/PHARMACIST SECTION

If irriation or discomfor occurs, please discontinue to use and consult a doctor/physician.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children and pets' reach.

Questions

OTC - QUESTIONS SECTION

Please contact us when you have any questions at service@utimi.com

Indications & usage

INDICATIONS & USAGE 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.

This product is not a contraceptive or spermicide.

Direction

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.

The active ingredient strength is 1.27% w/w.

Warnings

WARNINGS SECTION

  • If irriation or discomfort occurs, please 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

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82624-101-032023-07-28C16284748780-10191ceaa-6afe-198a-e063-dbdaa90aec3eWater Based Personal Lubricant, UTIMI, 30mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82624-101-03UTIMI water based personal lubricant30 mL in 1 BOTTLELOTION301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82624-101UTIMI WATER BASED PERSONAL LUBRICANT (PERSONAL LUBRICANT) LOTION [SHENZHEN GUANGDIAN TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20220321_da8173ef-70c3-5c58-e053-2995a90a7018.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
82624-10182624-101-03

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

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
da8173ef-70c4-5c58-e053-2995a90a7018da8173ef-70c3-5c58-e053-2995a90a70182022-03-19WarningsExact identifier
spl id: da8173ef-70c4-5c58-e053-2995a90a7018
spl set id: da8173ef-70c3-5c58-e053-2995a90a7018