Kontakt Hand Sanitizer

Manufacturer
Select Specialty Products | ABC Compounding Co., Inc.
Effective date
2018-01-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:05:27

Label at a glance#

ProductKontakt Hand Sanitizer
Active ingredientBENZETHONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

Drug Facts Box OTC-Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

benzethonium chloride USP 0.2%

Drug Facts Box OTC-Indications & Usage Section

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box OTC-Warnings Section

WARNINGS SECTION

For external use only

Drug Facts Box OTC-Purpose Section

OTC - PURPOSE SECTION

Antiseptic

Drug Facts Box-OTC When Using Section

OTC - WHEN USING SECTION

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box-OTC Stop Use Section

OTC - STOP USE SECTION

irritation and redness develop

Drug Facts Box-OTC Keep Out Of Reach Of Children Section

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box-OTC Dosage & Administration Section

DOSAGE & ADMINISTRATION SECTION

press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand

rub hands together until dry

wash hands with soap and water at earliest opportunity

Drug Facts Box-OTC Inactive Ingredient Section

INACTIVE INGREDIENT SECTION

water, glycerine, dimethicone, DMDM hydantoin, iodopropynl butylcarbamate, fragrance

Kontakt II Hand Sanitizer 6575 Drug Facts and Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Kontakt II Hand Sanitizer 6575 Drug Facts and Label

FDA-Initiated Inactive NDC Indexing#

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
67996-57567996-575-10, 67996-575-18, 67996-575-14, 67996-575-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
ff1fdc09-17cf-c559-e053-6294a90ac2b42bddb1c8-44cd-4668-a9b1-4237ed6df0602023-06-27WarningsExact identifier
spl set id: 2bddb1c8-44cd-4668-a9b1-4237ed6df060

Reported adverse events (FAERS/openFDA)#

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