WISH HAND SANITIZER ISLAND COCONUT- alcohol gel

WISH HAND SANITIZER ISLAND COCONUT by

Drug Labeling and Warnings

WISH HAND SANITIZER ISLAND COCONUT by is a Otc medication manufactured, distributed, or labeled by CLICK PRODUCTS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient:

Ethyl Alcohol 70% v/v

PURPOSE

Purpose

Antimicrobial

INDICATIONS & USAGE

USE: · Hand sanitizer to help reduce bacteria on the skin that may cause disease.

WARNINGS

Warnings: for external use only.

Flammable. Keep away from heat and flame.

WHEN USING

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

Stop use and ask a doctor if

· irritation or redness develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. if swallowed, get medical help or contact a poison control center.

DOSAGE & ADMINISTRATION

Directions

· spray enough product in your palm to thoroughly cover your hands.

· rub hands together briskly until dry. Recommended for repeated use.

· children under 6years of age should be supervised when using this product.

INACTIVE INGREDIENT

Inactive Ingredients: · Water(Aqua), Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate.

PRINCIPAL DISPLAY PANEL

ITEM#60350
Island Coconut
1.2 FL OZ. (35ml)
NDC: 71611-092-01

PRINCIPAL DISPLAY PANEL

ITEM#60351
Island Coconut
1.2 FL OZ. (35ml)
NDC: 71611-092-02

PRINCIPAL DISPLAY PANEL

ITEM#60352
Island Coconut
1.5 FL OZ. (45ml)
NDC: 71611-092-03

PRINCIPAL DISPLAY PANEL

ITEM#60353
Island Coconut
1.5 FL OZ. (45ml)
NDC: 71611-092-04

INGREDIENTS AND APPEARANCE

WISH HAND SANITIZER ISLAND COCONUT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71611-092
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71611-092-01	1 in 1 BAG	06/28/2024
1		35 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 71611-092-02	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/28/2024
3	NDC: 71611-092-03	1 in 1 BAG	06/28/2024
3		45 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 71611-092-04	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/28/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/28/2024

Labeler - CLICK PRODUCTS LLC (080766174)