SSDC MYSTIC FOAMING HAND SANITIZER- benzalkonium chloride solution

SSDC Mystic Foaming Hand Sanitizer by

Drug Labeling and Warnings

SSDC Mystic Foaming 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

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin
  

Warnings

• For external use only
  

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

• skin irritation or redness occurs for more than 72 hours
  

KEEP OUT OF REACH OF CHILDREN

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

Directions

• wash hands to remove soil
• dispense palmful
• spread to cover hands, rub in well
• air dry, do not rinse or towel dry
  

Other information

• for additional information, see Safety Data Sheet (SDS)
• for emergency medical information in USA call 1-800-391-1504

INACTIVE INGREDIENT

Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, FD&C Red 40, FD&C Blue 1

Questions?

Call 1-800-532-7732

Principal display panel and representative container

SSDC

MYSTIC

Foaming Hand Sanitizer

Benzalkonium chloride 0.1%

Net Contents: 1250 mL/42.3 US fl oz

Distributed by:  SSDC Division, Kay Chemical Company

4050 Corporate Drive, #100

Grapevine, Texas 76051, USA 800.532.7732

INGREDIENTS AND APPEARANCE

SSDC MYSTIC FOAMING HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-674
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isopropyl alcohol (UNII: ND2M416302)
Propylene glycol (UNII: 6DC9Q167V3)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-674-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/17/2025
2	NDC: 47593-674-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/17/2025

Labeler - Ecolab Inc. (006154611)