Label: DERMACIDE- benzalkonium chloride solution
- NDC Code(s): 11695-2158-6
- Packager: Butler Animal health Supply, LLC dba Covetrus North America
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 5, 2022
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- STATEMENT OF IDENTITY
- WARNINGS AND PRECAUTIONS
- HOW SUPPLIED
- Indications:
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Directions:
Soak affected area liberally with Dermacide solution. Apply daily until hair begins to grow. Leave treated areas uncovered. Rinse treated areas with clear water before reapplying. Results should be apparent in a matter of days. If no improvement is noted within seven days, consult your veterinarian.
- Caution:
- Active ingredient:
- Other ingredients:
- Warning:
- Note:
- Storage:
- INFORMATION FOR OWNERS/CAREGIVERS
- 16 fl oz (473 mL)
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INGREDIENTS AND APPEARANCE
DERMACIDE
benzalkonium chloride solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:11695-2158 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 3.09 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11695-2158-6 12 in 1 CASE 1 473 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2013 Labeler - Butler Animal health Supply, LLC dba Covetrus North America (603750329) Establishment Name Address ID/FEI Business Operations First Priority, Incorpporated 179925722 manufacture, api manufacture, label