ANTIMICROBIAL FOAM

Manufacturer
Sky Systems Co., Inc
Effective date
2022-04-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:44:45

Label at a glance#

ProductANTIMICROBIAL FOAM
Active ingredientCHLOROXYLENOL
Label structure9 sections

Indications and uses

HELPS PREVENT CROSS CONTAMINATION BY HAND CONTACT TO REDUCE INCIDENCE ON NOSOCOMIAL INFECTION.

Dosage and administration

WET HANDS AND FOREARMS. APPLY A SMALL AMOUNT OF SOAP AND SCRUB THOROUGHLY FOR 1 MINUTE. RINSE THOROUGHLY. DRY HANDS COMPLETELY.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

CHLOROXYLENOL 0.45%

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

HELPS PREVENT CROSS CONTAMINATION BY HAND CONTACT TO REDUCE INCIDENCE ON NOSOCOMIAL INFECTION.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. AVOID ANY FOODS CONTAMINATION DURING APPLICATION AND STORAGE.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IN CASE OF CONTACT WITH EYES FLUSH THOROUGHLY WITH WATER.

AVOID CONTACT WITH BROKEN SKIN.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

WET HANDS AND FOREARMS. APPLY A SMALL AMOUNT OF SOAP AND SCRUB THOROUGHLY FOR 1 MINUTE. RINSE THOROUGHLY. DRY HANDS COMPLETELY.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, SODIUM LAURETH SULFATE, PROPYLENE GLYCOL, POLYQUATERNIUM 7, FRAGRANCE, CITRIC ACID, FD&C YELLOW #5 (CAS #1934-21-0), FD&C rED #4 (CAS #548-53-2), D&C RED #33 (CAS #567-66-6), FD&C BLUE #1 (CAS #3844-15-9).

OTHER SAFETY INFORMATION

CHEMICAL EMERGENCY #: 1-800-255-3924

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antimicrobial Foam Soap LabelAntimicrobial Foam Soap Label

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67106-723167106-7231-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
1aa4b4ee-90d2-0186-e063-6394a90a1a7e68900b98-3d5e-633e-e053-2a91aa0a2a982024-06-11WarningsExact identifier
spl set id: 68900b98-3d5e-633e-e053-2a91aa0a2a98

Reported adverse events (FAERS/openFDA)#

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