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

Warnings

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

Do not use
on children less than 2 months of age
on open skin wounds

When using this product keep out of eyes, ears, and mouth. In
case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may
be signs of a serious condition.

Directions

Place enough product on hands or affected area to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Uses

Antiseptic and Hand Sanitizer to help reduce bacteria that may cause disease. For use when soap & water are unavailable.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Inactive ingredient

Water

Other information

Store between 15 °C and 30 °C. Avoid freezing and excessive heat above 400 °C (104 °F)

Product label

INGREDIENTS AND APPEARANCE

BENEMAX ADVANCED HAND SANITIZER 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73700-004
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
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73700-004-01	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/25/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/25/2021

Labeler - Nugale Pharmaceutical Inc (202595872)

Establishment
Name	Address	ID/FEI	Business Operations
Nugale Pharmaceutical Inc		202595872	manufacture(73700-004)