HAND SANITIZER- ethyl alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Luminary Distilling, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Warnings

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

Active ingredients

Active ingredient[s] Purpose

Alcohol 76.95% Antiseptic

Do not use

Do not use

* in children less than 2 months of age

* on open skin wounds

When using this product

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

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

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Inactive ingredients

Inactive ingredients purified water USP (21.025%), isopropyl alcohol (4.95%), glycerin (1.875%), hydrogen peroxide (0.15%)

Other information

Other information

* Store between 15-30C (59-86F)

* Avoid freezing and excessive heat above 40C (104F)

Use[s]

Use[s]

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

Directions

Directions

* 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.

Purpose

Purpose

Antiseptic

Luminary Distilling Liquid Hand Sanitizer

Liquid Hand Sanitizer

Non-Sterile Solution

Alcohol Antiseptic 76.95%

Topical Solution

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73888-101
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
GLYCERIN (UNII: PDC6A3C0OX)	1.875 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.15 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	21.025 mL  in 100 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302)	4.95 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73888-101-02	750 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	03/24/2020
2	NDC: 73888-101-03	118.294 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/24/2020
3	NDC: 73888-101-01	18927.059 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/24/2020

Labeler - Luminary Distilling, LLC (058432986)

Registrant - Luminary Distilling, LLC (058432986)

Establishment
Name	Address	ID/FEI	Business Operations
Luminary Distilling, LLC		058432986	manufacture(73888-101)