INSTANT HAND SANITIZER- alcohol gel

Instant hand sanitizer by

Drug Labeling and Warnings

Instant hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Naftali Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

USES

For hand sanitizing to decrease bacteria on skin.

WARNINGS

Flammable. Keep away fire or flame.

For external use only. Keep out of eyes. If eye contact occured, flush immediately with water and call a doctor. Stop use and ask a doctor if irritation develops.

KEEP OUT OF REACH OF CHILDREN

Call a doctor or Poison Center if swallowed.

DIRECTIONS

Apply a pea sized amount onto your hand, and rub throughly until dry.

Use as needed. For children under 6, use with adult supervision.

INACTIVE INGREDIENTS

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

500 mL NDC: 75819-001-01

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75819-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETOL (UNII: Q4R969U9FR)
WATER (UNII: 059QF0KO0R)
CHAMOMILE (UNII: FGL3685T2X)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75819-001-01	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - Naftali Inc (832036268)