FDA.reportPublic FDA data

Sujanils WOW Instant Hand Sanitiser

Manufacturer
Sujanil Chemo Industries
Effective date
2020-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:35

Label at a glance#

ProductSujanils WOW Instant Hand Sanitiser
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Sujanil's WOW Instant Hand Sanitiser

SPL UNCLASSIFIED SECTION

WOW Instant Hand Sanitiser Kills 99.9% germs Instantly

a. Alcohol (Ethanol) (70%, volume/volume(v/v).

b. Glycerol (0.5% v/v).

c. Aloe vera (0.5% v/v)

d. Sterile distilled water or Boiled cold water.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic, Antimicrobial, Hand Sanitizer

Purpose

OTC - PURPOSE SECTION

Antiseptic, Antimicrobial, Hand Sanitiser

Use

INDICATIONS & USAGE SECTION

WOW Instant Hand Sanitiser to help reduce bacteria that potentially can cause disease. For use soap and water are not available

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

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Isopropyl Alcohol, Aloe vera leaf extract, Neem, Glycerol, Propylene glycol, Carbomer, Triethanolamine, Fragrance(Parfum)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

000 mL NDC: 76441-909-__

Front LabelFront 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
76441-999-182022-01-28C16284748780-1d6a99b39-c712-a426-e053-dadaa90af4c2Sujanil's WOW Instant Hand Sanitiser
76441-999-812022-01-28C16284748780-1d6a99b39-c712-a426-e053-dadaa90af4c2Sujanil's WOW Instant Hand Sanitiser
76441-999-902022-01-28C16284748780-1d6a99b39-c712-a426-e053-dadaa90af4c2Sujanil's WOW Instant Hand Sanitiser

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76441-999-18Sujanils WOW Instant Hand Sanitiser236 mL in 1 BOTTLE, PUMPGEL2361
76441-999-81Sujanils WOW Instant Hand Sanitiser100 mL in 1 BOTTLEGEL1001
76441-999-90Sujanils WOW Instant Hand Sanitiser50 mL in 1 BOTTLEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76441-999SUJANILS WOW INSTANT HAND SANITISER (ALOCHOL) GEL [SUJANIL CHEMO INDUSTRIES]1Legacy NDC, 3 package rows20200813_acadf278-0c43-3fa7-e053-2a95a90a279c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76441-99976441-999-18, 76441-999-81, 76441-999-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
AZADIRACHTA INDICA SEED OIL4DKJ9B3K2TIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
acadf278-0c44-3fa7-e053-2a95a90a279cacadf278-0c43-3fa7-e053-2a95a90a279c2020-08-12WarningsExact identifier
spl id: acadf278-0c44-3fa7-e053-2a95a90a279c
spl set id: acadf278-0c43-3fa7-e053-2a95a90a279c

Reported adverse events (FAERS/openFDA)#

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