VIRIDIPHARM HAND SANITIZER ANTIBACTERIAL- alcohol gel

Viridipharm Hand Sanitizer Antibacterial by

Drug Labeling and Warnings

Viridipharm Hand Sanitizer Antibacterial by is a Otc medication manufactured, distributed, or labeled by Viridipharm, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% v/v

Purpose

Antimicrobial

Use

• Hand sanitizer to help reduce bacteria on the skin that could cause disease
• Recommended for repeated use

Warnings

Flammable. Keep away from fire or flame.

For external use only.

WHEN USING

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

STOP USE

Stop use and ask a doctor if irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Place enough product in your palm to thoroughly cover your hands.
• Rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product.

Other information

• Store below 110 F (43 C)
• May discolor certain fabrics or surfaces

Inactive ingredients

Aloe Barbadensis Leaf Juice (Aloe Vera), Carbomer, Glycerin, Sodium Hydroxide, Water

Questions or comments?

Call 609.733.5663

Monday through Friday 8:00 AM to 5:00 PM

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

VIRIDIPHARM HAND SANITIZER ANTIBACTERIAL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73267-001
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73267-001-08	236.6 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/13/2020
2	NDC: 73267-001-20	591.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/13/2020

Labeler - Viridipharm, LLC (081072201)