Alpha Handrub

Manufacturer: Alpha Cleantech Labs Inc
Effective date: 2020-05-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:14:16

Label at a glance#

ProductAlpha Handrub

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F) • sealed cap

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75 %

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin

• recommended for repeated use

• for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use

• in children less than 2 months of age

• on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop

• condition persists for more than 72 hours

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

• wet hands thoroughly with product and allow to dry without wiping

• supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30°C (59-86°F)

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

• sealed cap

INACTIVE INGREDIENT SECTION

Inactive ingredients glycerin, hydrogen peroxide, water

Questions? +1-877-962-2636

OTC - QUESTIONS SECTION

You may also report serious side effects to this phone number.

Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Manufactured for: Alpha Cleantech Labs Inc., Unit 111 – 20351 Duncan Way, Langley, British Columbia, V3A 7N3

COUNTRY OF ORIGIN : CANADA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1047755	ethanol 75 % Topical Solution	PSN	1
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	1
1047755	ethanol 75 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77959-075-01	2023-01-30	C162847	48780-1	f386c649-f3a4-0266-e053-dadaa90a7c1a	ALPHA HANDRUB ANTISEPTIC HAND SANITIZER
77959-075-05	2023-01-30	C162847	48780-1	f386c649-f3a4-0266-e053-dadaa90a7c1a	ALPHA HANDRUB ANTISEPTIC HAND SANITIZER
77959-075-50	2023-01-30	C162847	48780-1	f386c649-f3a4-0266-e053-dadaa90a7c1a	ALPHA HANDRUB ANTISEPTIC HAND SANITIZER
77959-075-60	2023-01-30	C162847	48780-1	f386c649-f3a4-0266-e053-dadaa90a7c1a	ALPHA HANDRUB ANTISEPTIC HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
77959-075-01	Alpha Handrub	3785 mL in 1 BOTTLE, PLASTIC	LIQUID	3785	1
77959-075-05	Alpha Handrub	18927 mL in 1 CONTAINER	LIQUID	18927	1
77959-075-50	Alpha Handrub	500 mL in 1 BOTTLE, PLASTIC	LIQUID	500	1
77959-075-60	Alpha Handrub	60 mL in 1 BOTTLE, PLASTIC	LIQUID	60	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77959-075	ALPHA HANDRUB (ETHYL ALCOHOL) LIQUID [ALPHA CLEANTECH LABS INC]	1	Legacy NDC, 4 package rows	20200522_c19aeb80-2f5b-401e-80ed-63886cfaafc1.zip

Products#

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

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

Alpha Handrub
Ethyl alcohol
ALCOHOL
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77959-075	77959-075-60, 77959-075-50, 77959-075-01, 77959-075-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	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
3e4116fa-76e8-40ec-80a8-5a533db5c3e5			c19aeb80-2f5b-401e-80ed-63886cfaafc1	2020-05-19	Warnings	Exact identifier spl id: 3e4116fa-76e8-40ec-80a8-5a533db5c3e5 spl set id: c19aeb80-2f5b-401e-80ed-63886cfaafc1

Reported adverse events (FAERS/openFDA)#

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