ANTISEPTIC WASH- 0.130% benzalkonium antiseptic wash liquid

Antiseptic Wash by

Drug Labeling and Warnings

Antiseptic Wash by is a Otc medication manufactured, distributed, or labeled by Swiss-American CDMO, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Warnings

For external use only. Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center right away. Do not use on deep or puncture wounds, animal bites or serious burns

Use and Directions

First aid to help prevent infection in minor cuts, scrapes and burns.

Use on adults and children 2 years and older. Use to clean minor cuts, scrapes and burns by thoroughly flushing the affected area. Let air dry. Cover with an adhesive bandage or sterile gauze. Use no more than 2 times daily. Children under 2 years of age: ask a doctor.

Keep out of reach of children

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Active Ingredient

Benzalkonium Chloride 0.130%

PURPOSE

Inactive Ingredient

Aloe Barbadensis Leaf Juice, Disodium EDTA, Poloxamer 188, Purified Water, Sodium Chloride, Sodium Citrate

Labeling

INGREDIENTS AND APPEARANCE

ANTISEPTIC WASH 
0.130% benzalkonium antiseptic wash liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60232-0022
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 g  in 1000 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POLOXAMER 188 (UNII: LQA7B6G8JG)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60232-0022-8	240 g in 1 BOTTLE; Type 0: Not a Combination Product	09/05/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/05/2013

Labeler - Swiss-American CDMO, LLC (080170933)

Registrant - Swiss-American CDMO, LLC (080170933)

Establishment
Name	Address	ID/FEI	Business Operations
Swiss-American CDMO, LLC		080170933	manufacture(60232-0022)