EA INSTANT HAND SANITIZER- alcohol gel

EA INSTANT HAND SANITIZER by

Drug Labeling and Warnings

EA INSTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by National Travel Product, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses 

• 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

• Pump appropriate amount of sanitizer on to hands and rub together until dry. Use as needed. For children under 6, use with adult supervison. Not recommended for infants.

Inactive ingredients:

Water, Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine.

Package Labeling: 300ml

Package Labeling: 500ml

Package Labeling:60ml

Package Labeling:120ml

Package Labeling:2L

INGREDIENTS AND APPEARANCE

EA INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78233-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75   in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
EDETOL (UNII: Q4R969U9FR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78233-013-00	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
2	NDC: 78233-013-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
3	NDC: 78233-013-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
4	NDC: 78233-013-03	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2020
5	NDC: 78233-013-04	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/14/2020

Labeler - National Travel Product, Inc (784475725)