MONK HAND SANITIZING WIPES- benzethonium chloride cloth

Monk by

Drug Labeling and Warnings

Monk by is a Otc medication manufactured, distributed, or labeled by National Towelette Company , National Towelette Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Principal Display Panel

MM1

ACTIVE INGREDIENT

Active Ingredients:
Benzethonium Chloride (0.3%)

PURPOSE

Purpose:

Antibacterial

DOSAGE & ADMINISTRATION

Use decreases bacteria on skin

WARNINGS

Warnings For external use only

DO NOT USE

Do not use

• over large areas
• If you are allergic to any of the ingredients
  

WHEN USING

When using this product

• do not get into eyes

If contact occurs, rinse thoroughly with water

STOP USE

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions: Adults and children 2 years and over: apply on hands and face to clean and refresh. Allow skin to dry without wiping. Children under 2 years: as a doctor before use. For Children under 6 use only under supervision.

INACTIVE INGREDIENT

Inactive Ingredients: Water, SD Alcohol 40-B, Sodium Benzoate, Diazolidinyl Urea, Glycerin, Propylene Glycol, Potassium Sorbate, Disodium EDTA, Tocopheryl Acetate, Aloe

STORAGE AND HANDLING

Store under 110 F

QUESTIONS

Questions and Comments: For products or technical information, contact National Towelette Monday to Friday 8 AM to 4 PM EST at 1-800-738-9068, or visit our website at www.towelettes.com

INGREDIENTS AND APPEARANCE

MONK  HAND SANITIZING WIPES
benzethonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50320-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzethonium Chloride (UNII: PH41D05744) (Benzethonium - UNII:1VU15B70BP)	Benzethonium Chloride	30 mL  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)	879 mL  in 1000 mL
Ethanol (UNII: 3K9958V90M)	111.60 mL  in 1000 mL
Sodium Benzoate (UNII: OJ245FE5EU)	1.30 mL  in 1000 mL
Diazolidinylurea (UNII: H5RIZ3MPW4)	1.30 mL  in 1000 mL
Glycerin (UNII: PDC6A3C0OX)	1.00 mL  in 1000 mL
Propylene Glycol (UNII: 6DC9Q167V3)	1.00 mL  in 1000 mL
Potassium Sorbate (UNII: 1VPU26JZZ4)	.75 mL  in 1000 mL
Edetate Disodium (UNII: 7FLD91C86K)	.45 mL  in 1000 mL
Alpha-Tocopherol Acetate (UNII: 9E8X80D2L0)	0.10 mL  in 1000 mL
Aloe (UNII: V5VD430YW9)	0.09 mL  in 1000 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50320-111-58	500 mL in 1 CANISTER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	01/06/2010

Labeler - National Towelette Company (782795041)

Registrant - National Towelette Company (782795041)

Establishment
Name	Address	ID/FEI	Business Operations
National Towelette Company		782795041	repack