COMMON SENSE- alcohol liquid

Common Sense by

Drug Labeling and Warnings

Common Sense by is a Otc medication manufactured, distributed, or labeled by Microbe Solutions, LLC, Whisk Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Ethanol 62%

PURPOSE

Purpose

Antimicrobial

INDICATIONS & USAGE

Uses

Hand sanitizer to help reduce bacteria on the skin

Recommended for repeated use

WARNINGS

Warnings

For external use only.

Flammable, keep away from fire and or flame.

When using this product do not use in or near eyes. In case of eye contact, flush thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and persists for more then 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control center right away.

DOSAGE & ADMINISTRATION

Directions

Dispense an adequate amount in your palm to cover all surfaces of hands completely

Rub hands together until dry.

Supervise children in the use of this product

STORAGE AND HANDLING

Other information

Do not store above 100 F (38 C)

May discolor some fabrics

INACTIVE INGREDIENT

Inactive ingredients

Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Citric Acid, 3-(trihydroxysilyl) propyldimethyloctadecyl ammonium chloride

QUESTIONS

Questions or comments?

Telephone: 1-833-7770-8320

Monday through Friday

8am till 5 pm EST

www.smartcommonsense.com

PRINCIPAL DISPLAY PANEL

Using Common Sense

Fine Mist Action

Provides Hours of Protection*

Common Sense

An Antimicrobial Solution

Fragrance-Free

Hand

Sanitizer

Kills 99.99% ofGerms

That Cause Illness

Cleans and Sanitizes

Will Not Wash Off

Enriched With Moisturizers

Eco-Friendly Formula

Clinically Tested  Non-Irritating

Meets CDC Requirements

for Hospital Use

1.7 fl. oz. (50 mL)

*Safely bonds to skin follicle-comes off naturally with exfoliation.

INGREDIENTS AND APPEARANCE

COMMON SENSE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72172-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72172-001-01	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/15/2018
2	NDC: 72172-001-02	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/15/2018
3	NDC: 72172-001-03	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/15/2018
4	NDC: 72172-001-04	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/15/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/15/2018

Labeler - Microbe Solutions, LLC (081104360)

Establishment
Name	Address	ID/FEI	Business Operations
Aire-Master of America, Inc.		057897381	manufacture(72172-001)