Instant Hand Sanitizer

Manufacturer
Zidac Laboratories Ltd
Effective date
2020-10-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:30:53

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer helps reduce bacteria on the skin Recommended for repeated use

Dosage and administration

Place product in palm of hand  Rub hands together until dry Supervise children under 6 years of age when using product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 77%v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer helps reduce bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or rash occurs and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place product in palm of hand 
  • Rub hands together until dry
  • Supervise children under 6 years of age when using product

Storage

SPL UNCLASSIFIED SECTION

Store below 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Carbomer, Aminomethyl Propanol, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, Propylene Glycol

Package Labeling: 100ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling: 500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:5000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1788839ethanol 77 % Topical GelPSN2
1788839ethanol 0.77 ML/ML Topical GelSCD2
1788839ethanol 77 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79699-000-032022-01-28C16284748780-1d6a99b39-95b4-a426-e053-dadaa90af4c2Instant Hand Sanitizer
79699-000-162022-01-28C16284748780-1d6a99b39-95b4-a426-e053-dadaa90af4c2Instant Hand Sanitizer
79699-000-192022-01-28C16284748780-1d6a99b39-95b4-a426-e053-dadaa90af4c2Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79699-000-03Instant Hand Sanitizer100 mL in 1 BOTTLEGEL1002
79699-000-16Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5002
79699-000-19Instant Hand Sanitizer5000 mL in 1 CANGEL50002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79699-000INSTANT HAND SANITIZER (ALCOHOL) GEL [ZIDAC LABORATORIES LTD]2Legacy NDC, 3 package rows20201003_ab70bc49-b5a0-cd46-e053-2a95a90a5ce7.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
79699-00079699-000-03, 79699-000-16, 79699-000-19

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
b0b4dadd-11da-3dbb-e053-2995a90a2097ab70bc49-b5a0-cd46-e053-2a95a90a5ce72020-10-02WarningsExact identifier
spl id: b0b4dadd-11da-3dbb-e053-2995a90a2097
spl set id: ab70bc49-b5a0-cd46-e053-2a95a90a5ce7

Reported adverse events (FAERS/openFDA)#

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