VITAL GEL ANTISEPTIC HAND SANITIZER- isopropyl alcohol gel

VITAL Gel ANTISEPTIC HAND SANITIZER by

Drug Labeling and Warnings

VITAL Gel ANTISEPTIC HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Ingersoll Products Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol 74% v/v

Purpose

Antiseptic

Uses

hand sanitizer to decrease bacteria on the skin recommended for repeated use for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame
For external use only

Do not use  in children less than 2 months of age on open skin wounds

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 7 2 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet hands thoroughly with product and allow to dry without wiping supervise children under 6 years when using this product to avoid swallowing

Other information

store between 15-30°C (59-86°F) avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

benzalkonium chloride, carbomer 940, glycerin, tetrahydroxypropyl ethylenediamine

Questions? +1-888-658-5515

You may also report serious side effects to this phone number.

Sun-Mon: 24 hours

REALTREE® Manufactured by: Ingersoll ProductsInc & Tetra Chem Industries Ltd,267 Ingersoll St S.Ingersoll, ON, Canada N5C 3J7 COUNTRY OF ORIGIN: CANADATO OPENTEAR    TWIST NPN 80099188

Packaging

INGREDIENTS AND APPEARANCE

VITAL GEL ANTISEPTIC HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80675-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	74 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
EDETOL (UNII: Q4R969U9FR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80675-010-98	1 in 1 BOX	11/11/2020
1		60 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/11/2020

Labeler - Ingersoll Products Inc (205147130)

Establishment
Name	Address	ID/FEI	Business Operations
Ingersoll Products Inc		205147130	repack(80675-010)