HAND SANITZER- hand sanitizer gel

Hand Sanitzer by

Drug Labeling and Warnings

Hand Sanitzer by is a Otc medication manufactured, distributed, or labeled by McConnell labs Inc, McConnell Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 80%

Purpose

Antiseptic

Uses

• ​To help reduce bacteria on the skin that potentially can cause disease
• Reccomended for repeated use

Warnings

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

Keep out of reach of childen

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

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.

Other Information

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

Inactive ingredients

Water (Aqua), Glycerin, Hydroxypropylcellulose

Questions?

Call us at +1 (541) 526-1417

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73991-679
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	17.4 mL  in 100 mL
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)	0.6 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73991-679-08	240 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020
2	NDC: 73991-679-02	59.147 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020
3	NDC: 73991-679-32	946.352 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/24/2020
4	NDC: 73991-679-04	118.29 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020
5	NDC: 73991-679-16	473.17 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/24/2020
6	NDC: 73991-679-01	3785 mL in 1 JUG; Type 0: Not a Combination Product	04/24/2020
7	NDC: 73991-679-05	18927 mL in 1 JUG; Type 0: Not a Combination Product	04/24/2020
8	NDC: 73991-679-55	208197 mL in 1 DRUM; Type 0: Not a Combination Product	04/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/25/2020

Labeler - McConnell labs Inc (061623240)

Establishment
Name	Address	ID/FEI	Business Operations
McConnell labs Inc		061623240	manufacture(73991-679)