SSDC ALPHASAN HAND SANITIZER- alcohol solution

SSDC Alphasan Hand Sanitizer by

Drug Labeling and Warnings

SSDC Alphasan Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethanol 60% by volume

Purpose

Antiseptic Handwash

Uses

• For handwashing to decrease bacteria on skin

Warnings

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

Do not use

• In eyes

When using this product

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

Stop use and ask a doctor if

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

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Other information

• 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

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

QUESTIONS

Questions?  call 1-800-532-7732

Principal display panel and representative label

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

INGREDIENTS AND APPEARANCE

SSDC ALPHASAN HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-680
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MYRISTYL ALCOHOL (UNII: V42034O9PU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-680-25	800 mL in 1 POUCH; Type 0: Not a Combination Product	12/31/2025
2	NDC: 47593-680-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/31/2025

Labeler - Ecolab Inc. (006154611)