MEDICAP HAND SANITIZER- alcohol solution

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]

Alcohol 80% v/v

Purpose

Antiseptic

Use[s]

Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

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 a serious condition.

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

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.

Other information

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT

Inactive ingredients: glycerin, hydrogen peroxide, distilled water

SPL UNCLASSIFIED SECTION

Topical Solution

Non-sterile Solution

Product of Canada

Distributed by:

Medicap Laboratories,

Tampa, FL 33610. +1-844-972-0220

Packaging

INGREDIENTS AND APPEARANCE

MEDICAP HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74126-080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	47.2 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: 74126-080-59	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/20/2020

Labeler - Zurich Pharma Inc (248184926)

Establishment
Name	Address	ID/FEI	Business Operations
Zurich Pharma Inc		248184926	manufacture(74126-080)