SANITIZE ASAP HAND SANITIZER- isopropyl alcohol gel

SANITIZE ASAP HAND SANITIZER by

Drug Labeling and Warnings

SANITIZE ASAP HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by New World Holdings, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient:

Isopropyl Alcohol 70%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses: to decrease bacteria on the skin that could interfere with good health, recommended for repeated use. 

WARNINGS

Warnings

Flammable, keep away from heat and flame.

Keep out of reach of children, keep out of the eyes, avoid contact with broken skin, if swallowed get medical help or contact a poison control center. 

DOSAGE & ADMINISTRATION

Directions: wet the hands thoroughly with the product and allow to dry without wiping.

INACTIVE INGREDIENT

Inactive Ingredients:

Alcohol, Deionized water, Hydroxypropyl guar, Eucalyptus globulus

SPL UNCLASSIFIED SECTION

ANTI-BACTERIAL

KILLS 99.99% OF GERMS

MADE IN USA

LABORATORY CRAFTED - ANTI-BACTERIAL BLEND FROM THE RESEARCH LABORATORIES OF NWH. 

BE SAFE  BE CAUTIOUS

SANITIZEASAP.COM

New World Cosmetics and Medicinals.

1080 Holland Drive. Suite 1

Boca Raton, Florida 33487

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat cure or prevent any disease.

Packaging

INGREDIENTS AND APPEARANCE

SANITIZE ASAP HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73871-377
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
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
GUARAPROLOSE (3500 MPA.S AT 1%) (UNII: 3A1I7376TC)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73871-377-60	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/18/2020
2	NDC: 73871-377-24	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/18/2020
3	NDC: 73871-377-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/18/2020
4	NDC: 73871-377-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/18/2020

Labeler - New World Holdings, Inc. (081183610)

Establishment
Name	Address	ID/FEI	Business Operations
New World Holdings, Inc.		081183610	manufacture(73871-377)