DAYCLEAR HAND SANITIZER GEL- ethyl alcohol liquid

DayClear Hand Sanitizer Gel by

Drug Labeling and Warnings

DayClear Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by GM Pharmaceuticals, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62% v/v

Purpose(s)

Antimicrobial

Use(s)

■ hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only.

Flammable. Keep away from fire or flame.

When using this product

do not use in or near the eyes.

In case of contact, rinse eyes thoroghyly with water.

Stop Use and Ask a Doctor if

Stop use and ask a doctor if irritation or rash appears and lasts

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children- If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ put enough product in your palm to cover all surfaces of both hands and rub hands together briskly until dry

■ children under 6 years should be supervised when using this product

Other Information

Store between 20-30ºC (68-86ºF)

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Carbomer, Chamomilla rectita (matricaria) flower extract, Diisopropylamine, Glycerin, Isopropyl myristate, Water

Questions?

Call 1-888-535-0305

PRINCIPAL DISPLAY PANEL

DayClear Hand Sanitizer Gel

NDC: 58809-226-02

2 fl.oz (59mL)

INGREDIENTS AND APPEARANCE

DAYCLEAR HAND SANITIZER GEL 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58809-226
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	550 g  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 980 (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58809-226-02	59 mL in 1 TUBE; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/30/2020

Labeler - GM Pharmaceuticals, Inc (793000860)