ANTISEPTIC HAND SANITIZER ALCOHOL FREE VALENCIA GROUP- benzalkonium chloride gel

Antiseptic Hand Sanitizer Alcohol Free Valencia Group by

Drug Labeling and Warnings

Antiseptic Hand Sanitizer Alcohol Free Valencia Group by is a Otc medication manufactured, distributed, or labeled by Midway Advanced Products, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Drug Facts

​Active ingredient

Benzalkonium chloride 0.13%

​Purpose

Antiseptic

​Use

• for handwashing to decrease bacteria on the skin

​Warnings

​For external use only

Do not use

• in the eyes

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

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

​Other information

• store at room temperature

butylene glycol, caesalpinia spinosa gum, citric acid, ethylhexylglycerin, fragrance, glycerin, phenoxyethanol, sodium lauryl sulfate, water

Hand Sanitizer 0.7mL

Hand Sanitizer 100 mL x 100 Carton

Hand sanitizer 100 mL

Hand Sanitizer Valencia

INGREDIENTS AND APPEARANCE

ANTISEPTIC HAND SANITIZER ALCOHOL FREE VALENCIA GROUP 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52490-501
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52490-501-03	0.7 mL in 1 PACKET; Type 0: Not a Combination Product	01/24/2018	04/10/2020
2	NDC: 52490-501-22	2000 in 1 CARTON	01/24/2018	04/10/2020
2		0.7 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 52490-501-40	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/24/2018	05/18/2020
4	NDC: 52490-501-23	100 in 1 CARTON	02/01/2018	05/18/2020
4		100 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/24/2018	05/18/2020

Labeler - Midway Advanced Products, LLC (962765009)