Vivacious Instant Hand Sanitizer

Manufacturer
Global 1 Wholesale Merchant Services, Inc. | GUANGZHOU ZUOFUN COSMETICS CO., LTD
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:13:13

Label at a glance#

ProductVivacious Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough amount of product on hands to cover all surface. Rub hands until dry. Supervise children under 6 years old when using this product to avoid swallowing.

Storage and handling

Store between 15 - 30°C (59 - 86°F) Avoid Freezing and Excessive Heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75 ± 5% (V/V)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To reduce bacteria on hand

Warnings

WARNINGS SECTION

For External Use Only

Flammable. Keep away from Heat or Flame

Do Not Use

OTC - DO NOT USE SECTION

In children less than 2 months of age

On open skin wounds

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctorif irritation or rash occur

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough amount of product on hands to cover all surface.

Rub hands until dry.

Supervise children under 6 years old when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store between 15 - 30°C (59 - 86°F)

Avoid Freezing and Excessive Heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Carbomer, Glycerol, Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL - NDC 77572-001-35

label-60mllabel-60ml

500 mL - NDC 77572-001-40

label-500mllabel-500ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN3
1305100ethanol 0.75 ML/ML Topical GelSCD3
1305100ethanol 75 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77572-001-352022-01-28C16284748780-1d6a99b39-d9fb-a426-e053-dadaa90af4c254d6bc04-c928-4c8e-bbb2-d1cb8d935259
77572-001-402022-01-28C16284748780-1d6a99b39-d9fb-a426-e053-dadaa90af4c254d6bc04-c928-4c8e-bbb2-d1cb8d935259

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77572-001-35Vivacious Instant Hand Sanitizer60 mL in 1 BOTTLE, PUMPGEL603
77572-001-40Vivacious Instant Hand Sanitizer500 mL in 1 BOTTLE, PUMPGEL5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77572-001VIVACIOUS INSTANT HAND SANITIZER (ALCOHOL) GEL [GLOBAL 1 WHOLESALE MERCHANT SERVICES, INC.]3Legacy NDC, 2 package rows20200516_54d6bc04-c928-4c8e-bbb2-d1cb8d935259.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77572-00177572-001-35, 77572-001-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
e9fe184e-2606-428b-95c5-53be2bf25b0454d6bc04-c928-4c8e-bbb2-d1cb8d9352592020-05-14WarningsExact identifier
spl id: e9fe184e-2606-428b-95c5-53be2bf25b04
spl set id: 54d6bc04-c928-4c8e-bbb2-d1cb8d935259

Reported adverse events (FAERS/openFDA)#

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