FDA.reportPublic FDA data

Watson Hand Sanitizer

Manufacturer
Tash Market Place
Effective date
2022-02-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:48:22

Label at a glance#

ProductWatson Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

When using this product

OTC - WHEN USING SECTION

rinse eyes thoroughly with water.

Stop use and ask a Doctor

OTC - STOP USE SECTION

if irritation and redness develop condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

SPL UNCLASSIFIED SECTION

  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Aminomethyl Propanol, Propylene Glycol, Tocopheryl Acetate, Barbadensis Leaf Extract, Fragrance (Parfun), Blue 1.

Package Labeling:59ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:237ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling:999ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90061-011-012023-07-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-022023-07-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-032023-07-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-042023-07-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-012022-02-21C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-022022-02-21C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-032022-02-21C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-042022-02-21C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-012022-01-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-022022-01-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-032022-01-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer
90061-011-042022-01-28C16284748780-1d6a99b39-5ee6-a426-e053-dadaa90af4c2Watson Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90061-011-01Watson Hand Sanitizer59 mL in 1 BOTTLEGEL592
90061-011-02Watson Hand Sanitizer237 mL in 1 BOTTLEGEL2372
90061-011-03Watson Hand Sanitizer500 mL in 1 BOTTLEGEL5002
90061-011-04Watson Hand Sanitizer999 mL in 1 BOTTLEGEL9992

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90061-011WATSON HAND SANITIZER (ALCOHOL) GEL [TASH MARKET PLACE]2Legacy NDC, 4 package rows20220222_ad2bbd34-5d87-b8a9-e053-2995a90acede.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
90061-01190061-011-01, 90061-011-02, 90061-011-03, 90061-011-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
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
d88f1711-bc3b-24fc-e053-2995a90a9bb6ad2bbd34-5d87-b8a9-e053-2995a90acede2022-02-21WarningsExact identifier
spl id: d88f1711-bc3b-24fc-e053-2995a90a9bb6
spl set id: ad2bbd34-5d87-b8a9-e053-2995a90acede

Reported adverse events (FAERS/openFDA)#

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