BENEMAX ADVANCED HAND SANITIZER- isopropyl alcohol liquid

BENEMAX ADVANCED Hand Sanitizer by

Drug Labeling and Warnings

BENEMAX ADVANCED Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Nugale Pharmaceutical Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 70%, USP

Purpose

Antiseptic

Uses

as a hand sanitizer when there is no water, to reduce bacteria on the skin which can cause illness. 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, or inhale
• in case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor

if a rash on irritation appear and remain at the site of contact

Keep out of reach of children.

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

Directions

• dispense sufficient liquid to cover the hands, rub hands together briskly for 30 seconds.

     Allow hands to dry.

children under 6 years of age must be upervised when using this product.

Other information

• do not store above 110 0F (43 0C). May discolor certain fabrics or substances

Inactive ingredient

Aloe (aloe barbadensis) Juice, D-alpha-tocopheryl Acetate, Glycerin, PEG, Water

Product Label

INGREDIENTS AND APPEARANCE

BENEMAX ADVANCED HAND SANITIZER 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73700-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73700-002-01	1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/15/2020

Labeler - Nugale Pharmaceutical Inc (202595872)

Establishment
Name	Address	ID/FEI	Business Operations
Nugale Pharmaceutical Inc		202595872	manufacture(73700-002)