FDA.reportPublic FDA data

Soft Care Impact Mini Instant Hand Sanitizer

Manufacturer
Diversey. Inc. | Kutol Products Company, Inc.
Effective date
2019-12-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:50:54

Label at a glance#

ProductSoft Care Impact Mini Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

for handwashing to decrease bacteria on the skin.

Recommended for repeat use.

WARNINGS SECTION

Warnings

For external use only.

Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use

in the eyes.

In case of eye contact, immediately flush with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or redness develop

condition persists 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.

DOSAGE & ADMINISTRATION SECTION

Directions

wet hands thoroughly with product

rub hands together covering all surfaces until hands are dry.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Glycerin, Carbomer, Triisopropanolamine, Propylene Glycol, Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

container label DSCIMDL2fcontainer label DSCIMDL2fcontainer label DSCIMDL2bcontainer label DSCIMDL2b

NDC 64536-1565-3

Diversey

SoftCare Impact Mini

Instant Hand Sanitizer

SDS # MS0301561

Net Contents

44.4 mL /

1.5 U.S. fl. oz.

SKU 100932937Manufactured for;

2018 Diversey, Inc., PO Box 19747

Charlotte, NC 28219-0747 U.S.A.

300200776 (18/052)

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
64536-156564536-1565-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)Z135WT9208IACT
TRIISOPROPANOLAMINEW9EN9DLM98IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL ALCOHOLND2M416302IACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB

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
2968b2c0-7406-8816-e063-6294a90a554084b6360c-8084-4689-aaa2-cf2f27fe8b012024-12-16WarningsExact identifier
spl set id: 84b6360c-8084-4689-aaa2-cf2f27fe8b01

Reported adverse events (FAERS/openFDA)#

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