PHARMAINT GEL HAND SANITIZER- ethyl alcohol 70% gel

Pharmaint Gel Hand Sanitizer by

Drug Labeling and Warnings

Pharmaint Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Laboratorio Pharma International Srl. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70%

­­­­­­­­­­­­­­­­­­­­­ Purpose

Antiseptic

Uses

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).

Inactive Ingredients

Water, Carbomer, triethanolamine, propylene glycol, glycerine, aloe vera, FD&C Yellow 5, FD&C Blue 1

Pharmaint Gel Hand Sanitizer

INGREDIENTS AND APPEARANCE

PHARMAINT GEL HAND SANITIZER 
ethyl alcohol 70% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73182-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	84 mL  in 120 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYACRYLIC ACID (300000 MW) (UNII: A8371R0U5J)
PROPYLENE GLYCOL ALGINATE (UNII: 26CD3J2R0C)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73182-101-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - Laboratorio Pharma International Srl (816365775)

Registrant - Laboratorio Pharma International Srl (816365775)