Vianor, Hand Sanitizer, 65% Alcohol, Gel, 60mL

Manufacturer
Shandong Vianor Healthy Science Co., Ltd. | A03 Lab of BTS
Effective date
2020-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:12

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Rua hands throughly with gel and let dry.

Storage and handling

Do not strore above 110℉/43℃.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep product away from open flames.

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use on children less than 2 months of age.

Do not use on open skin wounds.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes and broken skin.

In case of contact with eyes, rinse immediately with water.

OTC - STOP USE SECTION

If skin irritation occurs, discontinue use. Consult a doctor if rash persit.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and superise during use.

Directions

DOSAGE & ADMINISTRATION SECTION

Rua hands throughly with gel and let dry.

Other information

STORAGE AND HANDLING SECTION

Do not strore above 110℉/43℃.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, VE.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

6060

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN1
902574ethanol 0.65 ML/ML Topical GelSCD1
902574ethyl alcohol 65 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69980-101-032022-01-28C16284748780-1d6a99b39-c111-a426-e053-dadaa90af4c2Vianor, Hand Sanitizer, 65% Alcohol, Gel, 60mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69980-101-03Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69980-101HAND SANITIZER (65% ALCOHOL) GEL [SHANDONG VIANOR HEALTHY SCIENCE CO., LTD.]1Legacy NDC, 1 package rows20200522_a62b3596-b30d-2b0e-e053-2995a90a68dd.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69980-10169980-101-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT

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
a62b3596-b30e-2b0e-e053-2995a90a68dda62b3596-b30d-2b0e-e053-2995a90a68dd2020-05-21WarningsExact identifier
spl id: a62b3596-b30e-2b0e-e053-2995a90a68dd
spl set id: a62b3596-b30d-2b0e-e053-2995a90a68dd

Reported adverse events (FAERS/openFDA)#

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