FDA.reportPublic FDA data

WYANDOTTE SANIFECT E3-NA

Manufacturer
Alex C. Fergusson, Inc.
Effective date
2019-12-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:54:30

Label at a glance#

ProductWYANDOTTE SANIFECT E3-NA
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

USES HAND SANITIZER TO HELP REDUCE BACTERIA THAT POTENTIALLY CAN CAUSE DISEASES HELPS PREVENT CROSS CONTAMINATION BT HAND CONTACT HELPS PREVENT DRYING AND CHAFFING OF SKIN RECOMMENDED FOR REPEATED USE

Dosage and administration

DIRECTIONS: PUMP A SMALL AMOUNT OF FOAM INTO PALM OF HAND. RUB THOROUGHLY OVER ALL SURFACES OF BOTH HANDS. RUB HANDS TOGETHER BRISKLY UNTIL DRY. OTHER INFORMATION:  FOR FOOD PROCESSING, FOOD SERVICE AND PROFESSIONAL USE ONLY

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

DRUG FACTS

ACTIVE INGREDIENTS: BENZALKONIUM CHLORIDE 0.1%

PURPOSE SECTION

OTC - PURPOSE SECTION

ANTIMICROBIAL

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL INGESTION, SEEK MEDICAL ATTENTION OF CONTACT POISON CONTROL CENTER IMMEDIATELY.

INDICATIONS AND USES SECTION

INDICATIONS & USAGE SECTION

USES

HAND SANITIZER TO HELP REDUCE BACTERIA THAT POTENTIALLY CAN CAUSE DISEASES

HELPS PREVENT CROSS CONTAMINATION BT HAND CONTACT

HELPS PREVENT DRYING AND CHAFFING OF SKIN

RECOMMENDED FOR REPEATED USE

WARNINGS SECTION

WARNINGS: FOR EXTERNAL USE ONLY 

WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IN CASE OF EYE CONTACT, FLUSH EYES WITH WATER.

STOP USE AND ASK A DOCTOR IF IRRITATION OR REDNESS DEVELOPS, OR IF CONDITION PERSISTS FOR MORE THAN 72 HOURS.

DOSAGE AND ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: PUMP A SMALL AMOUNT OF FOAM INTO PALM OF HAND. RUB THOROUGHLY OVER ALL SURFACES OF BOTH HANDS. RUB HANDS TOGETHER BRISKLY UNTIL DRY.

OTHER INFORMATION:  FOR FOOD PROCESSING, FOOD SERVICE AND PROFESSIONAL USE ONLY

INACTIVE INGREDIENT SECTION

WATER, CETRIMONIUM CHLORIDE, LAURTRIMONIUM CHLORIDE, DIHYDROXYETHYL COCAMINE OXIDE, GLYCERETH-17 COCOATE

QUESTIONS OR COMMENTS

OTC - QUESTIONS SECTION

QUESTIONS OR COMMENTS: FOR PRODUCT OR TECHNICAL INFORMATION, CONTACT AFCO MONDAY TO FRIDAY 8 AM TO 4 PM EST AT 1-800-345-1329 OR VISIT OUR WEBSITE AT WWW.AFCOCARE.COM

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WYANDOTTE  #5581

SANIFECT E3-NA HAND SANITIZER

NDC# 68776-1003-2  CONTENTS: 4 X 1 GALLON

BATCH NO:

EXP DATE:

CONTENTS:

MANUFACTURED BY:

ALEX C. FERGUSSON

800 DEVELOPMENT AVENUE

CHAMBERSBURG, PA. 17201

TOLL FREE: 800 345-1329

CHEMTREC EMERGENCY 800-424-9300

(CHEMTREC CUSTOMER NUMBER: CCN837)

HMIS HAZARD RATING 

HEALTH 1  

FLAMMABILITY 0   

REACTIVITY   0  

PERSONAL PROTECTION   -

ALEX C. FERGUSSON

800 DEVELOPMENT AVENUE

CHAMBERSBURG, PA. 17201

TEL: 1-800-345-1329

alexferg_sanifect_E3_NAalexferg_sanifect_E3_NA

res

12 X 7 oz. bottle Case-Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5581 12-case 7oz btl5581 12-case 7oz btl

5581 7oz btl5581 7oz btl

res

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W72
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y2
CETRIMONIUM CHLORIDEINACTIVE INGREDIENTUC9PE95IBP2
DIHYDROXYETHYL COCAMINE OXIDEINACTIVE INGREDIENT8AR51R3BL52
GLYCERETH-17 COCOATEINACTIVE INGREDIENT3057VPT0KC2
LAURTRIMONIUM CHLORIDEINACTIVE INGREDIENTA81MSI0FIC2
WATERINACTIVE INGREDIENT059QF0KO0R2

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
68776-100368776-1003-2, 68776-1003-5

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
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-17 COCOATE3057VPT0KCIACT

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
5bdc128a-2e50-4e3b-bd2b-fb48c7db737c6da7f6f9-5392-4048-897f-3fcaab51ca822023-12-04WarningsExact identifier
spl set id: 6da7f6f9-5392-4048-897f-3fcaab51ca82

Reported adverse events (FAERS/openFDA)#

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