KEEP N IT CLEAN SANALL HAND SANITIZER FRESH SCENT- alcohol gel

Keep n It Clean Sanall Hand Sanitizer Fresh Scent by

Drug Labeling and Warnings

Keep n It Clean Sanall Hand Sanitizer Fresh Scent by is a Otc medication manufactured, distributed, or labeled by Sanall Enterprises, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient[s]

Alcohol 70% v/v

Purpose

Antiseptic

Use:

• Hand sanitizer to help reduce bacteria on the skin that potentally can cause disease.
• For use when soap and water are not available.

Warnings:

• For exeternal use only.
• Flammable. 
• Keep away from heat or flame.

Do not use

• in children less than 2 months of age. 
• on open skin wounds
• in eyes.

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 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 when using this product to avoid swallowing.

Other information

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

Inactive ingredients

acrylates copolymer, alpha-tocopherol acetate, denatonium benzoate, glycerin, isopropyl myristate, propylene glycol, tert-butyl alcohol, triisopropanolamine, fragrance.

Package Labeling:59ml

Package Labeling: 3785ml

INGREDIENTS AND APPEARANCE

KEEP N IT CLEAN SANALL HAND SANITIZER FRESH SCENT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79537-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79537-001-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/15/2020
2	NDC: 79537-001-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/15/2020

Labeler - Sanall Enterprises, LLC (117566912)