INSTANT HAND SANITIZER- hand sanitizer solution

Instant Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 70%

Purpose

Antibacterial

Use

For rinse-free hand sanitizing to remove 99.9% bacteria on skin.

Warnings

​Flammable. Keep away from fire or flame. For external use only.​

When using this product

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use and ask a doctor if

irritation and redness develop and persist.

Keep out of reach of children.

If swallowed, get medical health promptly

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Other Information

Store under 105°F

Inactive Ingredients

Aloe Barbadenisis Leaf, Glycerin, Hydroxypropylcellulose, Vitamin E, Water

PRINCIPAL DISPLAY PANEL

4 ounces (118 mL) - NDC: 00000-000-00

8 ounces (236 mL) - NDC: 00000-000-00

16 ounces (437 mL) - NDC: 00000-000-00

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
hand sanitizer solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73817-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73817-100-04	0.118 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/04/2020
2	NDC: 73817-100-08	0.236 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/04/2020
3	NDC: 73817-100-16	0.473 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/04/2020

Labeler - American Screening LLC (169065054)

Establishment
Name	Address	ID/FEI	Business Operations
American Screening LLC		169065054	manufacture(73817-100)