MYNT HAND SANITIZERS- ethyl alcohol gel

Mynt Hand Sanitizers by

Drug Labeling and Warnings

Mynt Hand Sanitizers by is a Otc medication manufactured, distributed, or labeled by Prive International Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

INDICATIONS & USAGE

Uses: To decrease bacteria on the skin that could cause disease  ▪ Recommended for repeated use.

WARNINGS

WARNINGS: For external use only: Hands.

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

When using this product ▪ Keep out of eyes. In case of contact with eyes, flush thoroughly with water

▪ Avoid contact with broken skin ▪ Do not inhale or ingest ▪ Stop use and ask a doctor if: irritation and

redness develop or condition persists for more than 72 hours.

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

DOSAGE & ADMINISTRATION

Directions: Wet hands thoroughly with product and allow to dry without wiping ▪ For children under 6,

use only under adult supervision ▪ Not recommended for infants.

STORAGE AND HANDLING

Other information: Do not store above 105°F ▪ May discolor some fabrics ▪ Harmful to wood finishes and plastics.

INACTIVE INGREDIENT

Inactive ingredients Deionized Water, Aloe Vera Gel (Aloe Barbadensis Leaf Juice), Carbomer, Triethanolamine,

Vitamin E (Tocopheryl Acetate).

SPL UNCLASSIFIED SECTION

70% ALCOHOL

Kills 99.99% of Germs

Aloe Vera & Vitamin E

Fragrance Free

*Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Distributed by: Mynt Brands Miami, FL 33179

www.myntsanitizers.com - Info@myntsanitizers.com

CRUELTY FREE

VEGAN

PARABEN FREE

NO SULFATES

MADE IN USA

Packaging

Packaging

INGREDIENTS AND APPEARANCE

MYNT HAND SANITIZERS 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79442-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79442-100-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
2	NDC: 79442-100-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020
3	NDC: 79442-100-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020
4	NDC: 79442-100-12	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020
5	NDC: 79442-100-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020
6	NDC: 79442-100-28	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/10/2020

Labeler - Prive International Inc. (058849652)

Establishment
Name	Address	ID/FEI	Business Operations
Prive International Inc.		058849652	manufacture(79442-100)