SNSNH6-4501 Antiseptic Topical Solution HAND SANITIZER Non-Sterile Solution

Manufacturer
Shotwell Hydrogenics, LLC
Effective date
2020-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:17

Label at a glance#

ProductSHSNH6-4501
Active ingredientALCOHOL
Label structure8 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#

Active ingredients(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Do not use 

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

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 for a doctor if irritation 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 Centre 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

deionized water, glycerin, carbomer, triethanolamine, fragrance

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73870-515-332022-01-28C16284748780-1d6a99b39-8b1b-a426-e053-dadaa90af4c2SNSNH6-4501 Antiseptic Topical Solution HAND SANITIZER Non-Sterile Solution

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73870-515-33SHSNH6-45011249 L in 1 CONTAINERSOLUTION12491

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73870-515SHSNH6-4501 (ETHYL ALCOHOL) SOLUTION [SHOTWELL HYDROGENICS, LLC]1Legacy NDC, 1 package rows20200508_aae9fb07-9e86-4aec-b97a-6eaad1c66943.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73870-51573870-515-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML · Source PDF

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
9bc4721a-0983-4fea-a23b-5df29205361baae9fb07-9e86-4aec-b97a-6eaad1c669432020-05-01WarningsExact identifier
spl id: 9bc4721a-0983-4fea-a23b-5df29205361b
spl set id: aae9fb07-9e86-4aec-b97a-6eaad1c66943

Reported adverse events (FAERS/openFDA)#

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