Hand Sanitizer by CN Pharma

Manufacturer: Canadian National Pharma Group Inc
Effective date: 2020-07-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:23:03

Label at a glance#

ProductHand Sanitizer by CN Pharma

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) Report any adverse reaction to the FDA Medwatch Adverse Event Reporting Program or to: info@cnpharmagroup.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 80% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame.

Do not use

in children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

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

Report any adverse reaction to the FDA Medwatch Adverse Event Reporting Program or to: info@cnpharmagroup.com

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Denatonium Benzoate, Water, Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039339	ethanol 80 % Topical Solution	PSN	1
1039339	ethanol 0.8 ML/ML Topical Solution	SCD	1
1039339	ethanol 80 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77536-002-01	2022-01-28	C162847	48780-1	d6a99b39-5e18-a426-e053-dadaa90af4c2	ec9f8d45-7742-4e7e-8648-108d90a54b77
77536-002-02	2022-01-28	C162847	48780-1	d6a99b39-5e18-a426-e053-dadaa90af4c2	ec9f8d45-7742-4e7e-8648-108d90a54b77
77536-002-03	2022-01-28	C162847	48780-1	d6a99b39-5e18-a426-e053-dadaa90af4c2	ec9f8d45-7742-4e7e-8648-108d90a54b77
77536-002-04	2022-01-28	C162847	48780-1	d6a99b39-5e18-a426-e053-dadaa90af4c2	ec9f8d45-7742-4e7e-8648-108d90a54b77

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
77536-002-01	Hand Sanitizer by CN Pharma	60 mL in 1 BOTTLE, PLASTIC	LIQUID	60	1
77536-002-02	Hand Sanitizer by CN Pharma	330 mL in 1 BOTTLE, PLASTIC	LIQUID	330	1
77536-002-03	Hand Sanitizer by CN Pharma	500 mL in 1 BOTTLE, PLASTIC	LIQUID	500	1
77536-002-04	Hand Sanitizer by CN Pharma	750 mL in 1 BOTTLE, PLASTIC	LIQUID	750	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77536-002	HAND SANITIZER BY CN PHARMA (ALCOHOL) LIQUID [CANADIAN NATIONAL PHARMA GROUP INC]	1	Legacy NDC, 4 package rows	20200729_ec9f8d45-7742-4e7e-8648-108d90a54b77.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Hand Sanitizer by CN Pharma
Alcohol
GLYCERIN
HYDROGEN PEROXIDE
DENATONIUM BENZOATE
WATER
MENTHA SPICATA OIL
EAST INDIAN LEMONGRASS OIL
LAVENDER OIL
TEA TREE OIL
EUCALYPTUS OIL
COCONUT OIL
ORANGE OIL
ALOE
.ALPHA.-TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77536-002	77536-002-01, 77536-002-02, 77536-002-03, 77536-002-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
WATER	059QF0KO0R	IACT
MENTHA SPICATA OIL	C3M81465G5	IACT
EAST INDIAN LEMONGRASS OIL	UP0M8M3VZW	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT
TEA TREE OIL	VIF565UC2G	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
COCONUT OIL	Q9L0O73W7L	IACT
ORANGE OIL	AKN3KSD11B	IACT
ALOE	V5VD430YW9	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	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
4d092537-1d11-4baa-89b4-fa97b99197f7			ec9f8d45-7742-4e7e-8648-108d90a54b77	2020-07-20	Warnings	Exact identifier spl id: 4d092537-1d11-4baa-89b4-fa97b99197f7 spl set id: ec9f8d45-7742-4e7e-8648-108d90a54b77

Reported adverse events (FAERS/openFDA)#

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