Covidizer Hand Sanitizer

Manufacturer: Covidizer, LLC
Effective date: 2020-12-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:34:48

Label at a glance#

ProductCovidizer Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not availble. recommended for repeated use.

Dosage and administration

pump as needed into your palms and thoroughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not availble.
recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

Do not apply around eyes.

Do not use

OTC - DO NOT USE SECTION

in ears & mouth.

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

pump as needed into your palms and thoroughly spread on both hands.
rub into skin until dry.

Other information

SPL UNCLASSIFIED SECTION

store at 20°C (68°F to 77°F).
may discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-40 Hydrogenated Castor Oil, Chloroxylenol, Carbomer, Trolamine.

Package Labeling:30ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Package Labeling:60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2

Package Labeling:237ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3

Package Labeling:1000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4

Package Labeling:2000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78715-000-01	2022-01-28	C162847	48780-1	d6a99b39-665c-a426-e053-dadaa90af4c2	Covidizer Hand Sanitizer
78715-000-02	2022-01-28	C162847	48780-1	d6a99b39-665c-a426-e053-dadaa90af4c2	Covidizer Hand Sanitizer
78715-000-03	2022-01-28	C162847	48780-1	d6a99b39-665c-a426-e053-dadaa90af4c2	Covidizer Hand Sanitizer
78715-000-04	2022-01-28	C162847	48780-1	d6a99b39-665c-a426-e053-dadaa90af4c2	Covidizer Hand Sanitizer
78715-000-05	2022-01-28	C162847	48780-1	d6a99b39-665c-a426-e053-dadaa90af4c2	Covidizer Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78715-000-01	Covidizer Hand Sanitizer	30 mL in 1 BOTTLE	GEL	30		1
78715-000-02	Covidizer Hand Sanitizer	60 mL in 1 BOTTLE	GEL	60		1
78715-000-03	Covidizer Hand Sanitizer	237 mL in 1 BOTTLE	GEL	237		1
78715-000-04	Covidizer Hand Sanitizer	1000 mL in 1 BOTTLE	GEL	1000		1
78715-000-05	Covidizer Hand Sanitizer	2000 mL in 1 BOTTLE	GEL	2000		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78715-000	COVIDIZER HAND SANITIZER (ALCOHOL) GEL [COVIDIZER, LLC]	1	Legacy NDC, 5 package rows	20201209_b5f7cfb2-293c-5f00-e053-2a95a90aae6d.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Covidizer Hand Sanitizer
ALCOHOL
WATER
POLYOXYL 40 HYDROGENATED CASTOR OIL
CHLOROXYLENOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78715-000	78715-000-01, 78715-000-02, 78715-000-03, 78715-000-04, 78715-000-05

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
WATER	059QF0KO0R	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
CHLOROXYLENOL	0F32U78V2Q	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

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
b5f7cacb-92bb-a6b7-e053-2a95a90aea02			b5f7cfb2-293c-5f00-e053-2a95a90aae6d	2020-12-08	Warnings	Exact identifier spl id: b5f7cacb-92bb-a6b7-e053-2a95a90aea02 spl set id: b5f7cfb2-293c-5f00-e053-2a95a90aae6d

Reported adverse events (FAERS/openFDA)#

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