MEDICAP HAND SANITIZER- isopropyl alcohol spray

MEDICAP HAND SANITIZER by

Drug Labeling and Warnings

MEDICAP HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Zurich Pharma Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

Isopropyl alcohol 75% v/v

Purpose

Antiseptic

INDICATIONS & USAGE

Use(s): Hand sanitizer help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

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

Do not use: In 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 serious condition.

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

DOSAGE & ADMINISTRATION

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

STORAGE AND HANDLING

Other Information: Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F).

INACTIVE INGREDIENT

Inactive Ingredients: Glycerin, hydrogen peroxide, purified water USP.

SPL UNCLASSIFIED SECTION

Isopropyl Alcohol Antiseptic 75%

Non-sterile Solution

Product of Canada

Packaging

INGREDIENTS AND APPEARANCE

MEDICAP HAND SANITIZER 
isopropyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74126-075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	44.69 mL  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74126-075-59	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020

Labeler - Zurich Pharma Inc (248184926)

Establishment
Name	Address	ID/FEI	Business Operations
Zurich Pharma Inc		248184926	manufacture(74126-075)