Label: CORTI DERM- hydrocortisone solution
- NDC Code(s): 58829-160-10
- Packager: FIRST PRIORITY INCORPORATED
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 15, 2022
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- INFORMATION FOR OWNERS/CAREGIVERS
- HYDROCORTISONE:
- BURROW'S SOLUTION:
- CONTRAINDICATION:
- INGREDIENTS:
- INACTIVE INGREDIENT
- DOSAGE:
- PRECAUTIONS:
- Net Contents:
- 1 oz (30 mL) Bottle/Case Label
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INGREDIENTS AND APPEARANCE
CORTI DERM
hydrocortisone solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:58829-160 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 10.2 mg in 1 mL ALUMINUM ACETATE (UNII: 80EHD8I43D) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ACETATE .73 mg in 1 mL ACETIC ACID (UNII: Q40Q9N063P) (ACETIC ACID - UNII:Q40Q9N063P) ACETIC ACID 0.624 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58829-160-10 12 in 1 CASE 1 30 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/01/2009 Labeler - FIRST PRIORITY INCORPORATED (179925722) Establishment Name Address ID/FEI Business Operations FIRST PRIORITY INCORPORATED 179925722 manufacture