HAND SANITIZER SINGLE USE- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Skymall Holdings LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 75%v/v

Purpose

Antiseptic

Uses

■ Hand Sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

■ on children less than 2 months of age ■ on open skin wounds

When using this product

keep out of eyes, ears, ears and mouth. In case of eye contact immediately flush eyes thoroughly with water

Stop use and ask a doctor

if irritation or rash occurs. These may be the signs of a serious condition.

Keep out of reach of children

In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.

Directions

■ Place enough product on hands to cover all surfaces. Rub hands together until dry. ■ Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

■ Store between 15º-30ºC (59º-89ºF) ■ Avoid freezing and excessive heat above 40ºC (104ºF) ■ May discolor fabrics or surfaces.

Inactive ingredients

Glycerin, Hydroxypropyl Cellulose, Water

Inner Package Label

Outer Package Label

Package Label

Package Label

Inner Package Label

Outer Package Label

INGREDIENTS AND APPEARANCE

HAND SANITIZER  SINGLE USE
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80230-007
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
WATER (UNII: 059QF0KO0R)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80230-007-02	100 in 1 BOX	09/01/2020
1	NDC: 80230-007-01	2 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 80230-007-08	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/10/2020
3	NDC: 80230-007-16	499 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/2020

Labeler - Skymall Holdings LLC (080000475)