CANDO Ultra Hand Sanitizer

Manufacturer
Fabrication Enterprises
Effective date
2020-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:27

Label at a glance#

ProductCANDO Ultra Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

●Put enough product in your palm to cover hands and rub hands briskly until dry. ●Children under 6 years of age should be supervised when using products.

Storage and handling

●Store below 104°F (40°C) ●Avoid freezing and excessive heat above 104°F (40°C) ●May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

WARNINGS SECTION

For external use only. Flammable.

Keep away from 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

WHEN USING THE PRODUCT do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR if irritation or rash occurs.

These may be signs of a serious condition.

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

●Put enough product in your palm to cover hands and rub hands briskly until dry.

●Children under 6 years of age should be supervised when using products.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

●Store below 104°F (40°C)

●Avoid freezing and excessive heat above 104°F (40°C)

●May discolor certain fabrics or surfaces

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aloe Vera, Carbomer Interpolymer (type B), Glycerin, Lemon oil, Triethanolamine, Water (Aqua)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51452-108-012024-01-30C16284748780-11030e364-fe7c-111a-e063-dadaa90a10e2CANDO Ultra Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51452-108-01CANDO Ultra Hand Sanitizer236 mL in 1 BOTTLE, PUMPGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51452-108CANDO ULTRA HAND SANITIZER (ALCOHOL) GEL [FABRICATION ENTERPRISES]1Legacy NDC, 1 package rows20200929_b06a13fb-eb6f-2222-e053-2995a90afca4.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
51452-10851452-108-01

Ingredients#

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

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

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
b069b772-568c-6560-e053-2995a90a5691b06a13fb-eb6f-2222-e053-2995a90afca42020-09-28WarningsExact identifier
spl id: b069b772-568c-6560-e053-2995a90a5691
spl set id: b06a13fb-eb6f-2222-e053-2995a90afca4

Reported adverse events (FAERS/openFDA)#

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