MEDPRIDE ANTIBACTERIAL HAND WASH- benzalkonium chloride liquid

MedPride Antibacterial Hand Wash by

Drug Labeling and Warnings

MedPride Antibacterial Hand Wash by is a Otc medication manufactured, distributed, or labeled by Shield Line LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%(w/w)

Purpose

Antibacterial

Uses

• For washing hand to decrease bacteria on the skin

Warnings

For external use only

When using this product

• Avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if

irritation and redness develops

Keep out of reach of children

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

Directions

pump onto wet hands, vigorously work into lather rinse thoroughly

other information

Store in a cool dry place below 104 F

Inactive Ingredients

Benzophenone-4, Benzyl Alcohol, CI 42090, Citric Acid, Cocamide DEA, Cocamidopropyl Betaine, Fragrance, Glycerin, Lauryl Glucoside, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Chloride, Sodium Laureth Sulfate, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEDPRIDE ANTIBACTERIAL HAND WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52410-8092
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
COCO DIETHANOLAMIDE (UNII: 92005F972D)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SULISOBENZONE (UNII: 1W6L629B4K)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52410-8092-1	400 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/04/2020

Labeler - Shield Line LLC (078518916)