DAYCLEAR HAND SANITIZER- ethyl alcohol gel

DayClear Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Purpose

Ethyl Alcohol 62% v/v...........................Antimicrobial

Use

■ hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. 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 and ask a doctor

if irritation or rash appears and lasts

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 of age should be supervised when using this product

Other information

■ store at 20-30°C (68-86°F)

Inactive ingredients

aloe barbadensis leaf juice, carbomer, chamomilla recutita (matricaria) flower extract, diisopropylamine, glycerin, isopropyl myristate, water

PRINCIPAL DISPLAY PANEL

NDC: 58809-225-02
DayClear
HAND
SANITIZER
GEL
2 FL OZ (59 mL)

PRINCIPAL DISPLAY PANEL

NDC: 58809-225-08
DayClear
HAND
SANITIZER
GEL
8 FL OZ (237 mL)

PRINCIPAL DISPLAY PANEL

NDC: 58809-225-32
DayClear
HAND
SANITIZER
GEL
32 FL OZ (946 mL)

Principle Display Panel

NDC: 58809-225-12

DayClear

HAND

SANITIZER

GEL

12 fl. oz. (355 mL)

INGREDIENTS AND APPEARANCE

DAYCLEAR HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58809-225
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CHAMOMILE (UNII: FGL3685T2X)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58809-225-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
2	NDC: 58809-225-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
3	NDC: 58809-225-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
4	NDC: 58809-225-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - GM Pharmaceuticals, INC (793000860)