CSI E3 HAND SANITIZER- alcohol liquid

CSI E3 Hand Sanitizer by

Drug Labeling and Warnings

CSI E3 Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Central Solutions Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol 70%

Purpose

Antiseptic

Uses

An effective antimicrobial hand cleanser for topical application

Recommended for repeated use

Reduces transient microorganisms on intact skin

Keep hands from drying out due to repeated uses

Warnings

For External Use Only.

Flammable, keep away from fire or opem flame

When using this product:

Avoid contact with eyes

In case of eye contact, flush with water for 15 minutes

Discontinue use and see a doctor if irritation occurs

Avoid contact with broken skin

Keep out of reach of children.

Directions

Wet hands thoroughly with product.

Allow to dry without wiping.

Use no water or towels

Other information

Not tested on animals

Inactive Ingredients

Purified Water, Glycerin

Questions?

Call 800-255-0262

PRINCIPAL DISPLAY PANEL

CSI

E3 Hand Sanitizer

For Hand Washing

to Decrease Bacteria

On The Skin

Net Contents:

18 oz (532 mL)

INGREDIENTS AND APPEARANCE

CSI E3 HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62654-139
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)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62654-139-01	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/09/2020
2	NDC: 62654-139-38	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/09/2020
3	NDC: 62654-139-37	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/09/2020
4	NDC: 62654-139-02	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/09/2020
5	NDC: 62654-139-94	208197 mL in 1 DRUM; Type 0: Not a Combination Product	07/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/09/2020

Labeler - Central Solutions Inc (007118524)

Registrant - Central Solutions Inc (007118524)

Establishment
Name	Address	ID/FEI	Business Operations
Central Solutions Inc		007118524	manufacture(62654-139)