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 ADVANCED PHARMACEUTICAL SERVICES, INC. DBA AFFORDABLE QUALITY PHARMACEUTICALS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 80%

Purpose

Antiseptic

Warnings

For external use only

Flammable. Keep away from fire, flame, or sparks

When using this product keep out of eyes, ears, and mouth.

In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears on the skin.

Uses

• Reduce bacteria on the skin.
• Recommended for repeated use

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Children under 6 years of age should be supervised by an adult when applying this product

Keep out of reach of children

 If swallowed, get medical help or contact a Poison Control Center right away

Other informatio

• Store between 15-30C (59-86F)
• May discolor certain fabrics or surfaces

Inactive Ingredient

Avocado oil, rosemary oil, glycerin, hydrogen peroxide, purified water USP

Product Labels

INGREDIENTS AND APPEARANCE

PREMIUM HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 13411-849
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	8 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
AVOCADO OIL (UNII: 6VNO72PFC1)
Glycerin (UNII: PDC6A3C0OX)
ROSEMARY OIL (UNII: 8LGU7VM393)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13411-849-02	60 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/20/2020
2	NDC: 13411-849-08	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/20/2020
3	NDC: 13411-849-16	473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/20/2020
4	NDC: 13411-849-37	3780 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/20/2020

Labeler - ADVANCED PHARMACEUTICAL SERVICES, INC. DBA AFFORDABLE QUALITY PHARMACEUTICALS (187498279)