CLEANOLOGY ADVANCED HAND SANITIZER- alcohol liquid

Cleanology Advanced Hand Sanitizer by

Drug Labeling and Warnings

Cleanology Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Southern Telecom, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

USE:

Hand sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from fire or flame.

For external use only, do not inhale or ingest.

Do not use

in, or near the eyes. In case of contact with eyes, rinse thoroughly with water.

Avoid contact with broken skin

Stop use and ask a doctor if 

irritation or rash develop and persist for more than 72 hours.

Keep out of reach of children.

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

Directions

• Wet hands thoroughly with product and allow to dry without wiping.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

Other information

• Store below 110°F (43°C)
• May discolor certain fabrics or surfaces

Inactive ingredients

Water, acrylate/C10-30, alkyl acrylate crosspolymer, benzophenone-4, fragrance, glycerin, tocopherol

Package Labeling:76546-000-01

Package Labeling:76546-000-02

Package Labeling:76546-000-03

Package Labeling:76546-000-04

INGREDIENTS AND APPEARANCE

CLEANOLOGY ADVANCED HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76546-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SULISOBENZONE (UNII: 1W6L629B4K)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76546-000-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
2	NDC: 76546-000-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
3	NDC: 76546-000-03	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
4	NDC: 76546-000-04	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - Southern Telecom, Inc. (169110033)