FDA.reportPublic FDA data

Platinum Hand Care Hand Sanitizer Gel

Manufacturer
Crown Products Company
Effective date
2021-12-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:19:30

Label at a glance#

ProductPlatinum Hand Care Hand Sanitizer Gel
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Dosage and administration

• Apply enough product in your palm to thoroughly cover your hands. • Rub hands together briskly until dry. • Children under 6 years of age should be supervised when using this product.

Storage and handling

• Store Between 15-30°C (59-86°F) • Avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNING

WARNINGS SECTION

Flammable. Keep away from fire or flame.

This product is intended for external use only.

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

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

• Apply enough product in your palm to thoroughly cover your hands.

• Rub hands together briskly until dry.

• Children under 6 years of age should be supervised when using this product.

Other Information

STORAGE AND HANDLING SECTION

• Store Between 15-30°C (59-86°F)

• Avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT SECTION

Inactive Ingredients glycerin, hydrogen peroxide, purified water USP, Hydroxyethyl Cellulose.

SPL UNCLASSIFIED SECTION

HAND SANITIZER GEL W/ MOISTURIZER

Exclusively Distributed by:

CROWN PRODUCTS

Hand Sanitizer Gel is a blend of isopropyl alcohol, hydrogen peroxide and emollients that leaves hands feeling clean, soft & refreshed.

• MEETS CURRENT CDC GUIDELINES FOR ISOPROPYL ALCOHOL CONTENT.

• Contains 70% Isopropyl Alcohol

• Recommended for daily use

• No water or paper towels needed

• No sticky residue

IMPORTANT: Young children must be supervised when using this product. Stop use and consult a doctor if irritation or rash appears/persists.

CONTAINS: 2-propanol (67-63-0), Water (7732-18-5), Glycerol (56-81-5), Hydrogen Peroxide, aqueous solution (7722-84-1), Hydroxyethyl Cellulose (9032-42-2).

CROWN JANITORIAL PRODUCTS

450 NEPPERHAN AVENUE

YONKERS, NY 10701-6601

(914) 968-2222

FAX: (914) 968-2567

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackagingPackaging

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80132-97680132-976-21, 80132-976-41, 80132-976-81, 80132-976-16, 80132-976-32, 80132-976-01, 80132-976-05, 80132-976-30, 80132-976-55

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302ACTIB
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT

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
cc9188e6-a0f9-4adc-906f-1fee5db695b913caadfb-73c3-48a9-b88f-3b183ccdedad2021-12-22WarningsExact identifier
spl id: cc9188e6-a0f9-4adc-906f-1fee5db695b9
spl set id: 13caadfb-73c3-48a9-b88f-3b183ccdedad

Reported adverse events (FAERS/openFDA)#

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