HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer 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(s)

Alcohol 70% Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

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

Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

ASK DOCTOR

irritation or rash occurs. These may be signs of a serious condition

KEEP OUT OF REACH OF CHILDREN

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)
• Avoid 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 SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73991-670
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)	0.6 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	27.4 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73991-670-02	59.147 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020
2	NDC: 73991-670-04	118.294 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020
3	NDC: 73991-670-08	248.588 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020
4	NDC: 73991-670-16	473.176 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/24/2020
5	NDC: 73991-670-01	3785.411 mL in 1 JUG; Type 0: Not a Combination Product	04/24/2020
6	NDC: 73991-670-05	18927 mL in 1 JUG; Type 0: Not a Combination Product	04/24/2020
7	NDC: 73991-670-55	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	03/30/2020

Labeler - McConnell Labs Inc (061623240)

Establishment
Name	Address	ID/FEI	Business Operations
McConnell Labs, Inc		061623240	manufacture(73991-670)