SSDC Alphasan Hand Sanitizer

Manufacturer
Ecolab Inc.
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:30:33

Label at a glance#

ProductSSDC Alphasan Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on skin

Dosage and administration

Apply liberal amount into hand Spread by rubbing hands together Rub to dryness with attention to area around nails and between fingers

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 60% by volume

Purpose

OTC - PURPOSE SECTION

Antiseptic Handwash

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on skin

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire or flame, heat, sparks and sources of static discharge.

Do not use

OTC - DO NOT USE SECTION

  • In eyes

When using this product

OTC - WHEN USING SECTION

  • If in eyes, rinse promptly and thoroughly with water
  • Discontinue use if irritation and redness develop

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • Eye or skin irritation or redness occurs for more than 72 hours

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

  • Apply liberal amount into hand
  • Spread by rubbing hands together
  • Rub to dryness with attention to area around nails and between fingers

Other information

REFERENCES SECTION

  • THIS PRODUCT IS NOT A SUBSTITUTE FOR HANDWASHING WITH SOAP AND WATER
  • for additional information, see Safety Data Sheet (SDS)
  • for emergency medical information in USA, call 1-800-391-1504

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

OTC - QUESTIONS SECTION

Questions?  call 1-800-532-7732

Principal display panel and representative label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SSDC ALPHASAN

Hand Sanitizer

Active Ingredient: Ethanol 60% by volume

1111141

Net Contents

1200 mL (40.6 US FL OZ)

SDS-NC-872, SDS-NJ-20007

Distributed by:

SSDC Division, Kay Chemical Company

4050 Corporate Drive #100

Grapevine, TX 76051, USA 800.532.7732

©2020 Kay Chemical Company.  All Rights Reserved Made in United States | Hecho en Estados Unidos

777178/7302/0920

representative labelrepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039483ethanol 60 % Topical SolutionPSN1
1039483ethanol 0.6 ML/ML Topical SolutionSCD1
1039483ethanol 60 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-680-25SSDC Alphasan Hand Sanitizer800 mL in 1 POUCHSOLUTION8001
47593-680-56SSDC Alphasan Hand Sanitizer1200 mL in 1 BOTTLE, PLASTICSOLUTION12001

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-68047593-680-25, 47593-680-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
SSDC Alphasan Hand SanitizerALCOHOLEcolab Inc.bbb0f924-3224-47f0-85b2-ebe024f8f9582025-12-31WarningsExact identifier
ndc (package): 47593-680-25
ndc (package): 47593-680-56
ndc (product): 47593-680
ndc11 (package): 47593068056
ndc11 (package): 47593068025
spl id: a051634a-b997-4602-addf-89305e3ac208
spl set id: bbb0f924-3224-47f0-85b2-ebe024f8f958

Reported adverse events (FAERS/openFDA)#

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