FDA.reportPublic FDA data

AOPAR Water Based Personal Lubricant

Manufacturer
Shenzhen ZhiHuiChuangXiang Technology Co., Ltd
Effective date
2021-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:38

Label at a glance#

ProductAOPAR 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 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

Aopar Water-based Personal Lubricant is a supplement for the nature lubrication of penis or vagina, intending to moisturize and enhance the ease and comfort of intimate sexual activity.

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

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

OTC - ASK DOCTOR SECTION

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

Ask doctor/pharmacist

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.

86-755-83286325 / services@aopar.com

Pregnancy or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Pregnant or breast feeding women shall follow doctor advice.

Indications & usage

INDICATIONS & USAGE SECTION

Aopar Water-based Personal Lubricant is a supplement for the nature lubrication of penis or vagina, intending to moisturize and enhance the ease and comfort of intimate sexual activity.

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 discomfor 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

Container Label_AoparContainer Label_Aopar

Product Linked Resources#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73000-226-202022-07-29C16284748780-1e4f33bdf-ad88-d8a0-e053-dadaa90a6e4eWater Based Personal Lubricant, Aopar, 30mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73000-226-20AOPAR Water Based Personal Lubricant30 mL in 1 BOTTLELOTION301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73000-226AOPAR WATER BASED PERSONAL LUBRICANT (PERSONAL LUBRICANT) LOTION [SHENZHEN ZHIHUICHUANGXIANG TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20210413_bfaf4973-71ac-7133-e053-2a95a90a32d7.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
73000-22673000-226-20

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
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
bfaf4973-71ad-7133-e053-2a95a90a32d7bfaf4973-71ac-7133-e053-2a95a90a32d72021-04-13WarningsExact identifier
spl id: bfaf4973-71ad-7133-e053-2a95a90a32d7
spl set id: bfaf4973-71ac-7133-e053-2a95a90a32d7

Reported adverse events (FAERS/openFDA)#

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