HILLYARD FOAMING INSTANT HAND SANITIZER- alcohol liquid

Hillyard Foaming Instant Hand Sanitizer by

Drug Labeling and Warnings

Hillyard Foaming 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% w/w

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 enough foam into palm of hand to cover both hands.
• 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, PEG-10 Dimethicone, Glycerine, Fragrance, Citric Acid, Vitamin E, Aloe Barbadensis Leaf Juice.

Package/Label Principal Display Panel

Hillyard
Foaming Instant Hand Sanitizer

HIL0041003

Affinity
Dispensing System

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

Label

INGREDIENTS AND APPEARANCE

HILLYARD FOAMING INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76402-410
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)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
GLYCERIN (UNII: PDC6A3C0OX)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76402-410-02	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/11/2012
2	NDC: 76402-410-03	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/07/2012
3	NDC: 76402-410-04	12 in 1 CARTON	04/20/2020
3		946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4	NDC: 76402-410-06	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/22/2012
5	NDC: 76402-410-82	414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/21/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/07/2012

Labeler - Hillyard GMP (969081483)

Establishment
Name	Address	ID/FEI	Business Operations
Hillyard GMP		969081483	MANUFACTURE(76402-410)