Water-based Personal Lubricant, ACVIOO 001

Manufacturer
Shenzhen Dikailong Technology Ltd
Effective date
2017-10-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:49

Label at a glance#

ProductWater-based Personal Lubricant, ACVIOO 001
Active ingredientBUTYLENE GLYCOL
Label structure16 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

butylene glycol (20%): 48g/package or 48mL/package

Inactive ingredient

INACTIVE INGREDIENT SECTION

Inactive ingredient:

water (77.52%): 186.048mL/package

hydroxyethylcellulose (1.6%): 3.84mL/package

polyethylene glycol 300000 (0.5%): 1.2mL/package

phenoxyethanol (0.3%): 0.72mL/package

chlorphenesin (0.08%): 0.192mL/package

Purpose

OTC - PURPOSE SECTION

It can achieve higher lubricantion, longer lubrication time and less dosage.

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

When using

OTC - WHEN USING SECTION

Virginal 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 tube 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

ACVIOO 001 is a water-based personal lubricant, for penile and/or vaginal application, intended to lubricate and moisturize, to enhance the ease and comfort of intimate sexual activity, help relieve virginal dryness, and supplement to the body's natural lubricant.

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

Dosage & administration

DOSAGE & ADMINISTRATION SECTION

One bottle of 240mL in one package.

Dosage forms & strengths

DOSAGE FORMS & STRENGTHS SECTION

The lubricant is like oil form.

A small amount one time, or reapply as needed or desired.

The active ingredient strength is 20%.

Warnings

WARNINGS SECTION

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

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

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Container Label

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Container LabelContainer Label

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Package Label

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Package LabelPackage Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.acvioo.com/ACVIOO Container Label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71847-2215-52021-01-29C16284748780-1ba0f9c33-558e-a910-e053-dadaa90a0b85Water-based Personal Lubricant, ACVIOO 001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71847-2215-5Water-based Personal Lubricant, ACVIOO 001240 mL in 1 BOTTLEOIL2401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71847-2215WATER-BASED PERSONAL LUBRICANT, ACVIOO 001 (PERSONAL LUBRICANT) OIL [SHENZHEN DIKAILONG TECHNOLOGY LTD]1Legacy NDC, 1 package rows20171030_5cac4425-2fc1-ebfb-e053-2991aa0aba04.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
71847-221571847-2215-5

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
5cac4425-2fb0-ebfb-e053-2991aa0aba045cac4425-2fc1-ebfb-e053-2991aa0aba042017-10-30WarningsExact identifier
spl id: 5cac4425-2fb0-ebfb-e053-2991aa0aba04
spl set id: 5cac4425-2fc1-ebfb-e053-2991aa0aba04

Reported adverse events (FAERS/openFDA)#

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