ADRIANA CLIP ON HAND SANITIZER- alcohol gel

ADRIANA CLIP ON HAND SANITIZER by

Drug Labeling and Warnings

ADRIANA CLIP ON HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by OSTL, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Uses

hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

WARNINGS

Flammable. Keep away from heat and flame.

When using this product

avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

irritation or redness develops.

Keep out of reach of children.

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

Directions

• wet hands thoroughly with product and rub into skin until dry.
• Children under 6 years of age should be supervised by an adult when using this product.

Inactive ingredients

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine, ( ALOE VERA FD&C Blue No.1, FD&C Yellow No.5)

SPL UNCLASSIFIED SECTION

Imported by: O.S.T.L. Inc

Made in P.R.C.

Distributed by: VERNON SALES. INC

www.ostltrade.com

Drug Facts

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ADRIANA CLIP ON HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69950-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69950-020-01	53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/31/2018

Labeler - OSTL, INC. (020117798)

Registrant - OSTL, INC. (020117798)