FDA.reportPublic FDA data

SSDC Mystic Foaming Hand Sanitizer

Manufacturer
Ecolab Inc.
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:26:01

Label at a glance#

ProductSSDC Mystic Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only

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

  • 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

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

Other information

REFERENCES SECTION

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

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

Call 1-800-532-7732

Principal display panel and representative container

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

representative labelrepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-674-41SSDC Mystic Foaming Hand Sanitizer750 mL in 1 BOTTLE, PLASTICSOLUTION7501
47593-674-59SSDC Mystic Foaming Hand Sanitizer1250 mL in 1 BOTTLE, PLASTICSOLUTION12501

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
47593-67447593-674-41, 47593-674-59

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Isopropyl alcoholND2M416302IACT
Propylene glycol6DC9Q167V3IACT
FD&C RED NO. 40WZB9127XOAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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 Mystic Foaming Hand SanitizerBENZALKONIUM CHLORIDEEcolab Inc.09899c40-6e4a-48a9-8d09-d374f6ab855f2025-12-17WarningsExact identifier
ndc (package): 47593-674-41
ndc (package): 47593-674-59
ndc (product): 47593-674
ndc11 (package): 47593067459
ndc11 (package): 47593067441
spl id: d90e2b59-f811-4f76-8fd6-9b041075e1e8
spl set id: 09899c40-6e4a-48a9-8d09-d374f6ab855f

Reported adverse events (FAERS/openFDA)#

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