FDA.reportPublic FDA data

BeSafe Hand Sanitizer

Manufacturer
Besafe Industries LLC | Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:18

Label at a glance#

ProductBeSafe Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adults supervision Not reommended for infants

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacterial on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

Do not use in the eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more then 72 hours

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

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adults supervision

Not reommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, carbomer, triethanolamine, glycerin, aloe barbadensis gel, propylene glycol, tocopheryl acetate (Vitamin E)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77693-001-012022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787
77693-001-022022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787
77693-001-032022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787
77693-001-042022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787
77693-001-052022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787
77693-001-062022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787
77693-001-072022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787
77693-001-082022-01-28C16284748780-1d6a99b39-90eb-a426-e053-dadaa90af4c28a485c56-6aae-4880-8cbc-555cdb5c5787

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77693-001-01BeSafe Hand Sanitizer30 mL in 1 BOTTLESOLUTION301
77693-001-02BeSafe Hand Sanitizer60 mL in 1 BOTTLESOLUTION601
77693-001-03BeSafe Hand Sanitizer100 mL in 1 BOTTLESOLUTION1001
77693-001-04BeSafe Hand Sanitizer237 mL in 1 BOTTLESOLUTION2371
77693-001-05BeSafe Hand Sanitizer500 mL in 1 BOTTLESOLUTION5001
77693-001-06BeSafe Hand Sanitizer1000 mL in 1 BOTTLESOLUTION10001
77693-001-07BeSafe Hand Sanitizer1800 mL in 1 BOTTLESOLUTION18001
77693-001-08BeSafe Hand Sanitizer3780 mL in 1 BOTTLESOLUTION37801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77693-001BESAFE HAND SANITIZER (ALCOHOL) SOLUTION [BESAFE INDUSTRIES LLC]1Legacy NDC, 8 package rows20200715_8a485c56-6aae-4880-8cbc-555cdb5c5787.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
77693-00177693-001-01, 77693-001-02, 77693-001-03, 77693-001-04, 77693-001-05, 77693-001-06, 77693-001-07, 77693-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB

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
aa6c668f-3082-30e9-e053-2a95a90a44a28a485c56-6aae-4880-8cbc-555cdb5c57872020-07-14WarningsExact identifier
spl id: aa6c668f-3082-30e9-e053-2a95a90a44a2
spl set id: 8a485c56-6aae-4880-8cbc-555cdb5c5787

Reported adverse events (FAERS/openFDA)#

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