PREMIUM HAND SANITIZER- alcohol liquid

PREMIUM HAND SANITIZER by

Drug Labeling and Warnings

PREMIUM HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by MD Science Lab LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol 80%

Purpose

Antimicrobial

Use

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

• For external use only.

• When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

• Stop use and ask a doctor if irritation or redness develops, or if 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.

Directions

• Dispense a small amount into palm of hand.
• Rub thoroughly over all surfaces of both hands.
• Rub hands together briskly until dry.

Inactive Ingredients

Deionized Water, Glycerin, Hydrogen Peroxide.

PRINCIPAL DISPLAY PANEL - 3.7 liter Bottle Label

M.D.
Science Lab
LLC

PREMIUM
hand
sanitizer

Kills 99.99% of Germs

moisturizes & softens skin

1 gal 128 fl oz 3.7 liter e

INGREDIENTS AND APPEARANCE

PREMIUM HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69898-801
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69898-801-03	88 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
2	NDC: 69898-801-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
3	NDC: 69898-801-12	354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
4	NDC: 69898-801-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
5	NDC: 69898-801-01	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
6	NDC: 69898-801-55	208197 mL in 1 DRUM; Type 0: Not a Combination Product	07/01/2020
7	NDC: 69898-801-27	1040988 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product	07/01/2020
8	NDC: 69898-801-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	07/01/2020

Labeler - MD Science Lab LLC (054484289)