Freshorize Alcohol Free Foaming Hand Sanitizer

Manufacturer: Freshorize Ltd | Freshorize USA LLC
Effective date: 2020-06-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:49

Label at a glance#

ProductFreshorize Alcohol Free Foaming Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

To decrease bacteria on the skin.

Dosage and administration

Liberally apply product to sin by gently massaging until absorbed. Supervise children in the use of this product.

Contacts and useful links#

Websitewww.freshorize.com

www.freshorize.com

Label contents#

Full prescribing information#

Uses:

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use in eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor is skin irritation develops.

If ingested, get medical help or contact a Poison Control Center immediately.

Warnings:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions:

INSTRUCTIONS FOR USE SECTION

Liberally apply product to sin by gently massaging until absorbed.
Supervise children in the use of this product.

Other Information:

OTHER SAFETY INFORMATION

Avoid extreme temperatures.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), PEG-40 Hydrogenated Castor Oil, Parfum, Aloe Barbadensis Leaf Extract

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Benzalkonium Chloride

Purpose

OTC - PURPOSE SECTION

Antibacterial.

Product / Brand Name Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Free Foam Hand Sanitizer Label

Freshorize Alcohol Free Hand Sanitizer

DOSAGE & ADMINISTRATION SECTION

Requires no water or towels.
Apply small amounts to hands and rub lightly until dry.

www.freshorize.com

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52305-600-10	2022-01-28	C162847	48780-1	d6a99b39-74a2-a426-e053-dadaa90af4c2	Alcohol Free Foam Hand Sanitizer
52305-600-16	2022-01-28	C162847	48780-1	d6a99b39-74a2-a426-e053-dadaa90af4c2	Alcohol Free Foam Hand Sanitizer
52305-600-20	2022-01-28	C162847	48780-1	d6a99b39-74a2-a426-e053-dadaa90af4c2	Alcohol Free Foam Hand Sanitizer
52305-600-24	2022-01-28	C162847	48780-1	d6a99b39-74a2-a426-e053-dadaa90af4c2	Alcohol Free Foam Hand Sanitizer
52305-600-25	2022-01-28	C162847	48780-1	d6a99b39-74a2-a426-e053-dadaa90af4c2	Alcohol Free Foam Hand Sanitizer
52305-600-27	2022-01-28	C162847	48780-1	d6a99b39-74a2-a426-e053-dadaa90af4c2	Alcohol Free Foam Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
52305-600-10	Freshorize Alcohol Free Foaming Hand Sanitizer	100 mL in 1 BOTTLE, PUMP	LOTION	100	1
52305-600-16	Freshorize Alcohol Free Foaming Hand Sanitizer	160 mL in 1 BOTTLE, PUMP	LOTION	160	1
52305-600-20	Freshorize Alcohol Free Foaming Hand Sanitizer	280 mL in 1 BOTTLE, PUMP	LOTION	280	1
52305-600-24	Freshorize Alcohol Free Foaming Hand Sanitizer	240 mL in 1 BOTTLE, PUMP	LOTION	240	1
52305-600-25	Freshorize Alcohol Free Foaming Hand Sanitizer	250 mL in 1 BOTTLE, PUMP	LOTION	250	1
52305-600-27	Freshorize Alcohol Free Foaming Hand Sanitizer	270 mL in 1 BOTTLE, PUMP	LOTION	270	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52305-600	FRESHORIZE ALCOHOL FREE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LOTION [FRESHORIZE LTD]	1	Legacy NDC, 6 package rows	20200616_a8240952-4d78-3d99-e053-2a95a90a5329.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Freshorize Alcohol Free Foaming Hand Sanitizer
Benzalkonium Chloride
HYDROGENATED CASTOR OIL
DMDM HYDANTOIN
GLYCERIN
BENZALKONIUM
WATER
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52305-600	52305-600-10, 52305-600-20, 52305-600-27, 52305-600-25, 52305-600-16, 52305-600-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
GLYCERIN	PDC6A3C0OX	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a8240952-4d79-3d99-e053-2a95a90a5329			a8240952-4d78-3d99-e053-2a95a90a5329	2020-06-15	Warnings	Exact identifier spl id: a8240952-4d79-3d99-e053-2a95a90a5329 spl set id: a8240952-4d78-3d99-e053-2a95a90a5329

Reported adverse events (FAERS/openFDA)#

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