IZOD SALTWATER HAND SANITIZER- alcohol spray

Izod Saltwater Hand Sanitizer by

Drug Labeling and Warnings

Izod Saltwater Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Shalom International Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Alcohol Denat. 60%

Purpose

Antibacterial

Uses

• Hand sanitizer to help reduce bacteria on the skin that could cause disease. 
• Recommended for repeated use.

Warnings

• Flamable. Keep away from fire or flame.
• For external use only.

When using this product

• do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use & ask a doctor if

• irritation or rash appears & lasts.

Keep out of reach of children.

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

Directions

• Apply enough product to thoroughly cover hands.
• Rub hands together briskly until dry.

Other Information

• Do not store above 110°F (43°C).
• May discolor certain fabrics or surfaces.

Inactive Ingredients

Water / Aqua, PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, DMDM Hydantoin, Fragrance(Parfum), Sodium Hydroxide, Tocopheryl Acetate

Questions?

• Call 212-391-6970

Package Labeling:

INGREDIENTS AND APPEARANCE

IZOD SALTWATER HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73025-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
DMDM HYDANTOIN (UNII: BYR0546TOW)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73025-002-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2020

Labeler - Shalom International Corp (001384825)