SANI HANDS- ethyl alcohol gel

sani hands by

Drug Labeling and Warnings

sani hands by is a Otc medication manufactured, distributed, or labeled by Maine Craft Distilling, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 72%

Purpose

Antiseptic

Uses

Hand Sanitizer to help reduce bacteria on the skin that can cause disease.

Directions

Apply liberally to front and back of hands.

Allow to dry. Recommended for repeat use.

Warnings

For external use only: hands

Flammable, keep away from fire or flame.

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness appears and lasts.

Do not use on children less than 2 months of age and on open wounds. Do not inhale or ingest.

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

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

Other information

Store between 0ºC (32ºF) - 41ºC (105ºF)

Inactive ingredients

Methylcellulose, water, Fragrance

Customer Service

+1 800 960 4814

SPL UNCLASSIFIED SECTION

MADE IN USA

*INSTANTLY KILLS 99.99% OF TESTED GERMS

72% ALCOHOL

Triclosan Sulfate and Paraben free

*Eliminates 99.99% of tested germs, bacteria and viruses in as little as 15 seconds.

WWW.SANI-LABS.COM   

Packaging

INGREDIENTS AND APPEARANCE

SANI HANDS 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79359-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79359-001-16	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/17/2020

Labeler - Maine Craft Distilling, LLC (079283895)

Establishment
Name	Address	ID/FEI	Business Operations
Maine Craft Distilling, LLC		079283895	manufacture(79359-001)