AMCON LABS HAND SANITIZER LIGHT CLEANSING- alcohol spray

Amcon Labs Hand Sanitizer Light Cleansing by

Drug Labeling and Warnings

Amcon Labs Hand Sanitizer Light Cleansing by is a Otc medication manufactured, distributed, or labeled by Nomax, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 60% v/v

Purpose

Skin Sanitizer

Use

To help reduce the amount of bacteria on skin

Warnings

Flammable. Keep away from fire or flame.

For external use only. If swallowed, seek medical attention.

When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

Keep out of reach of children.

Directions

• Dispense a small amount of spray onto the hands.
• Spread on hands and rub into skin until dry.
• Dispense a smaller amount in one hand and spread over both hands and wrists.
• Rub into skin until dry.
• Children should be supervised while using this product.

Inactive Ingredient

Water, Glycerin, Propylene Glycol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMCON LABS HAND SANITIZER LIGHT CLEANSING 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51801-779
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	600 mL  in 1 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white (water white - colorless, dispensed as a spray)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51801-779-08	0.237 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/04/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/04/2023

Labeler - Nomax, Inc. (103220273)