HILLYARD INSTANT HAND SANITIZER- ethyl alcohol gel

Hillyard Instant Hand Sanitizer by

Drug Labeling and Warnings

Hillyard Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Hillyard GMP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use.

Warnings

For External Use Only.

Flammable. Keep away from fire or flame.

When using this product

avoid contact with eyes. In case of eye contact, flush eyes thoroughly with water.

Stop use and ask a doctor if

irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

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

Directions

• Pump small amount into palm of hand.
• Rub thoroughly over all surfaces of both hands.
• Rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

Water, Acrylates/C10-C30 Alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine, Glycerine, Fragrance, Citric Acid, Vitamin E, Aloe Barbadensis Leaf Juice.

Package/Label Principal Display Panel

Hillyard
Instant Hand
Sanitizer Gel

HIL0040203

affinity

Place cartridge into dispenser, label facing back, and gently push pump into receiver until it clicks into place.

To remove the cartridge and pump, rotate the green ring clockwise and pull the pump out.

HILLYARD INDUSTRIES
PO Box 909,
St. Joseph, MO
64502-0909 U.S.A.
Telephone: 816-233-1321
www.hillyard.com

NET CONTENTS 33.8 FL. OZ. 1L

HIL0040203
0216
PEEL HERE

Label

INGREDIENTS AND APPEARANCE

HILLYARD INSTANT HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76402-402
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)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
EDETOL (UNII: Q4R969U9FR)
GLYCERIN (UNII: PDC6A3C0OX)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76402-402-06	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/23/2012
2	NDC: 76402-402-03	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/21/2012
3	NDC: 76402-402-02	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/2013
4	NDC: 76402-402-83	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/2013
5	NDC: 76402-402-44	119 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/21/2012

Labeler - Hillyard GMP (969081483)

Establishment
Name	Address	ID/FEI	Business Operations
Hillyard GMP		969081483	MANUFACTURE(76402-402)