PLATINUM HAND CARE HAND SANITIZER GEL

Platinum Hand Care Hand Sanitizer Gel by

Drug Labeling and Warnings

Platinum Hand Care Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Crown Products Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PLATINUM HAND CARE HAND SANITIZER GEL- isopropyl alcohol gel 
Crown Products Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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PLATINUM HAND CARE HAND SANITIZER GEL

Drug Facts

Active Ingredient

Isopropyl Alcohol 70% v/v

Purpose

Antiseptic

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

WARNING

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.

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

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

Store Between 15-30°C (59-86°F)

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

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

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

PLATINUM HAND CARE HAND SANITIZER GEL 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80132-976
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80132-976-21	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2020	12/29/2023
2	NDC: 80132-976-41	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2020	12/29/2023
3	NDC: 80132-976-81	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2020	12/29/2023
4	NDC: 80132-976-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2020	12/29/2023
5	NDC: 80132-976-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2020	12/29/2023
6	NDC: 80132-976-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2020	12/29/2023
7	NDC: 80132-976-05	18925 mL in 1 CONTAINER; Type 0: Not a Combination Product	08/24/2020	12/29/2023
8	NDC: 80132-976-30	113550 mL in 1 CONTAINER; Type 0: Not a Combination Product	08/24/2020	12/29/2023
9	NDC: 80132-976-55	208180 mL in 1 CONTAINER; Type 0: Not a Combination Product	08/24/2020	12/29/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/24/2020	12/29/2023

Labeler - Crown Products Company (013419569)

Revised: 12/2021

Document Id: cc9188e6-a0f9-4adc-906f-1fee5db695b9

34390-5

Set id: 13caadfb-73c3-48a9-b88f-3b183ccdedad

Version: 2

Effective Time: 20211222