CLEAR HANI-TIZER- alcohol liquid

CLEAR Hani-tizer by

Drug Labeling and Warnings

CLEAR Hani-tizer by is a Otc medication manufactured, distributed, or labeled by PHARMAPACKS, LLC, Central Solutions Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol 70%

Purpose

Hand Sanitizer

Uses

An antiseptic hand sanitizer for topical application.

Helps prevent infection and cross-contamination.

Reduces transient microorganisms on intact skin.

Recommended for repeated use.

Warnings

For external use only

Flammable, keep away from fire or flame.

When using this product avoid contact with eyes.

In case of eye contact, flush with water 15 minutes.

Discontinue use and see a doctor if irritation occurs.

Avoid contact with broken skin.

Keep out of reach of children.

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

Directions

Wet hands thoroughly with product.

Allow to dry without wiping.

Use no water or towels.

Inactive ingredients

Purified Water, Carbomer, Isopropanol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopherol (Vitamin E), Isopropyl Myristate, Diisopropyl Sebacate, Propylene Glycol, Aminomethyl Propanol, Fragrance, Yellow 5, Blue 1.

Questions?

Call 1-855-797-2257

PRINCIPAL DISPLAY PANEL

CLEAR

The Choice Is Clear

HANI-TIZER

Germ Barrier

purpose:

germ assassin

scent:

fresh

benefits:

easy to use

one-handed application

quick drying hand sanitizer

nourishing aloe + vitamin E

8 Fl.Oz. 237 mL

A Brand By PHARMAPACKS

INGREDIENTS AND APPEARANCE

CLEAR HANI-TIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73599-002
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
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TOCOPHEROL (UNII: R0ZB2556P8)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73599-002-08	237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/22/2020

Labeler - PHARMAPACKS, LLC (079254738)

Establishment
Name	Address	ID/FEI	Business Operations
Central Solutions Inc		007118524	manufacture(73599-002)