CURAD GERM SHIELD- benzethonium chloride liquid

Curad Germ Shield by

Drug Labeling and Warnings

Curad Germ Shield by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzethonium Chloride 0.1%

Purpose

First Aid Antiseptic

Uses

for first aid to help prevent infection in

• minor cuts
• scrapes
• burns

Warnings

For external use only.

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

When using this product

• do not use in or near the eyes
• do not apply over large areas of the body or in large quantities
• do not use longer than 1 week unless directed by a doctor

Stop use and ask doctor if

• condition worsens
• symptoms persist for more than 7 days, or clear up and occur again within a few days

Keep out of reach of children.

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

Directions

• Clean affected area
• Adjust nozzle and spray a small amount of this product on the area 1 to 3 times daily
• If used as a wet compress, keep bandage wet with solution
• If covered with a sterile bandage, let dry first

Inactive ingredients

Citric Acid, Cocamidopropyl Betaine, Disodium Phosphate, Phenoxyethanol, Water.

Label

INGREDIENTS AND APPEARANCE

CURAD GERM SHIELD 
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-093
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-093-08	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/02/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/02/2019

Labeler - Medline Industries, Inc. (025460908)

Establishment
Name	Address	ID/FEI	Business Operations
Swiss-American CDMO, LLC		080170933	manufacture(53329-093)