INSTANT HAND SANITIZER- alcohol gel

Instant Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

DRUG FACTS

Active Ingredient

Ethyl Alcohol 77%v/v

Purpose

Antimicrobial

Uses

• Hand sanitizer helps reduce bacteria on the skin
• Recommended for repeated use

Warnings

Flammable. Keep away from fire or flame. For external use only.

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor 

if irritation or rash occurs and lasts.

Keep out of reach of children.

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

Directions

• Place product in palm of hand 
• Rub hands together until dry
• Supervise children under 6 years of age when using product

Storage

Store below 110°F (43°C)

Inactive ingredients

Water (Aqua), Glycerin, Carbomer, Aminomethyl Propanol, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, Propylene Glycol

Package Labeling: 100ml

Package Labeling: 500ml

Package Labeling:5000ml

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79699-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.77 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79699-000-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020
2	NDC: 79699-000-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020
3	NDC: 79699-000-19	5000 mL in 1 CAN; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2020

Labeler - Zidac Laboratories Ltd (222761253)