Santotizer

Manufacturer
Santolubes LLC
Effective date
2021-04-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:40:05

Label at a glance#

ProductSantotizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

Alcohol 80% v/v

OTC - ACTIVE INGREDIENT SECTION

1.3oz1.3oz3600 ml label3600 ml label

DOSAGE & ADMINISTRATION SECTION

Directions

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.

WARNINGS SECTION

Warnings

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

INACTIVE INGREDIENT SECTION

Inactive ingredients glycerin, hydrogen peroxide, purified water

INDICATIONS & USAGE SECTION

Use[s]

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

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.

OTC - PURPOSE SECTION

Purpose

Antiseptic

changed label

RECENT MAJOR CHANGES SECTION

Changed label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3,600ml NDC 73976-1330-1

18,000ml NDC 73976-1330-2

200,000ml NDC 73976-1330-3

1,022,000ml NDC 73976-1330-4 3600ml3600ml 18000ml18000ml 200000ml200000ml 1022000ml1022000ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN4
1039339ethanol 0.8 ML/ML Topical SolutionSCD4
1039339ethanol 80 % Topical SolutionSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73976-1330-1Santotizer3.6 L in 1 PAILLIQUID3.64
73976-1330-2Santotizer18 L in 1 PAILLIQUID184
73976-1330-3Santotizer200 L in 1 DRUMLIQUID2004
73976-1330-4Santotizer1022 L in 1 TANKLIQUID10224
73976-1330-6Santotizer0.0384456 L in 1 BOTTLE, SPRAYLIQUID0.03844564

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73976-1330SANTOTIZER (HAND SANTIZER SOLUTION) LIQUID [SANTOLUBES LLC]4Legacy NDC, 5 package rows20210430_a18cef50-abdf-a416-e053-2a95a90a83de.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73976-133073976-1330-3, 73976-1330-1, 73976-1330-2, 73976-1330-4, 73976-1330-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
c11f0d97-8e5b-1dfe-e053-2a95a90a8c3ea18cef50-abdf-a416-e053-2a95a90a83de2021-04-29WarningsExact identifier
spl id: c11f0d97-8e5b-1dfe-e053-2a95a90a8c3e
spl set id: a18cef50-abdf-a416-e053-2a95a90a83de

Reported adverse events (FAERS/openFDA)#

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