FDA.reportPublic FDA data

SnoSan Hand Sanitizer

Manufacturer
J AND L DISTILLING COMPANY
Effective date
2020-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:41

Label at a glance#

ProductSnoSan Hand Sanitizer
Active ingredientALCOHOL
Label structure14 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#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

​Alcohol 80% v/v. Purpose: Antiseptic

SnoSan Drug FactsSnoSan Drug Facts

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Drug Facts PurposeDrug Facts Purpose

Use

INDICATIONS & USAGE SECTION

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

UseUse

Warnings

WARNINGS SECTION

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

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

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds

Do Not UseDo Not Use

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.

When usingWhen using

OTC - STOP USE SECTION

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

Stop useStop use

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.

Out of reachOut of reach

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.

DirectionsDirections

Other information

STORAGE AND HANDLING SECTION

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

StorageStorage

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Inactive IngredientsInactive Ingredients

RECENT MAJOR CHANGES SECTION

added image

Full Label - Front and BackFull Label - Front and Back

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 74283-0001-6

[SnoSan Logo]

Alcohol Antiseptic 80%

WHO Recommended Hand Rub Formula

Hand Sanitizer

Topical Solution

Non-sterile Solution

NET WT: 1 Gallon (3.785L)

J AND L DISTILLING COMPANY [logo]

4843 PEARL ST

BOULDER, CO 80301

CONTACT US: SnoSan@jldistilling.com

Front LabelFront Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74283-0001-12022-01-28C16284748780-1d6a99b39-eefe-a426-e053-dadaa90af4c2a22a3635-8c68-3184-e053-2995a90a644b
74283-0001-22022-01-28C16284748780-1d6a99b39-eefe-a426-e053-dadaa90af4c2a22a3635-8c68-3184-e053-2995a90a644b
74283-0001-32022-01-28C16284748780-1d6a99b39-eefe-a426-e053-dadaa90af4c2a22a3635-8c68-3184-e053-2995a90a644b
74283-0001-42022-01-28C16284748780-1d6a99b39-eefe-a426-e053-dadaa90af4c2a22a3635-8c68-3184-e053-2995a90a644b
74283-0001-52022-01-28C16284748780-1d6a99b39-eefe-a426-e053-dadaa90af4c2a22a3635-8c68-3184-e053-2995a90a644b
74283-0001-62022-01-28C16284748780-1d6a99b39-eefe-a426-e053-dadaa90af4c2a22a3635-8c68-3184-e053-2995a90a644b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74283-0001-1SnoSan Hand Sanitizer700 mL in 1 BOTTLE, PLASTICLIQUID7001
74283-0001-2SnoSan Hand Sanitizer500 mL in 1 BOTTLE, PLASTICLIQUID5001
74283-0001-3SnoSan Hand Sanitizer473 mL in 1 BOTTLE, PLASTICLIQUID4731
74283-0001-4SnoSan Hand Sanitizer118 mL in 1 BOTTLE, PLASTICLIQUID1181
74283-0001-5SnoSan Hand Sanitizer59 mL in 1 BOTTLE, PLASTICLIQUID591
74283-0001-6SnoSan Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICLIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74283-0001SNOSAN HAND SANITIZER (ALCOHOL) LIQUID [J AND L DISTILLING COMPANY]1Legacy NDC, 6 package rows20200402_a22a3635-8c68-3184-e053-2995a90a644b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74283-000174283-0001-1, 74283-0001-2, 74283-0001-3, 74283-0001-4, 74283-0001-5, 74283-0001-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
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
a22a30e7-18c9-2794-e053-2995a90a067ba22a3635-8c68-3184-e053-2995a90a644b2020-03-31WarningsExact identifier
spl id: a22a30e7-18c9-2794-e053-2995a90a067b
spl set id: a22a3635-8c68-3184-e053-2995a90a644b

Reported adverse events (FAERS/openFDA)#

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