Skip to Content

Excel Hydrocortisone

Generic Name: hydrocortisone lotion
Dosage Form: FOR ANIMAL USE ONLY

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Facts

Active Ingredient

0.5% Hydrocortisone Base, U.S.P


Uses

  • Provides soothing relief from itching caused by inflamation, seborrheic dermatitits, insect bites and other minor skin irritations
  • For use on dogs and cats

Relieves Itching

Helps Soothe Skin Irritations

Fast Acting, Long Lasting Relief

Non-Stinging


Warnings

  • For animal use only
  • Not for use on animals intended for consumption

Cautions

  • Do not use in the eyes or nose
  • Not for prolonged use
  • Do not apply to large areas of the body
  • Do not use where infection (pus) is present, since the drug may allow infection to be spread
  • If redness, irritation, or swelling persists or increases, discontinue use and consult your veterinarian

Directions

  • Apply lotion directly to affected skin areas
  • Do not use more than 3-4 times daily

other Information

Store at 20-25C (68-77F)

Other Ingredients

Aloe Vera Gel, Cetearyl Alcohol, Citric Acid, Diazolidinyl Urea, Glycerin, Glyceryl Monostearate, Isopropy Myristate, Methylparaben, Polysorbate 20, Propylparaben, Sodium Cetearyl Sulfate, Sodium Lauryl Sulfate, Water.

EXCEL 
hydrocortisone lotion lotion
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:24730-802
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYDROCORTISONE (HYDROCORTISONE) HYDROCORTISONE 0.59 g  in 118 g
Inactive Ingredients
Ingredient Name Strength
GLYCERIN  
ALOE VERA LEAF  
DIAZOLIDINYL UREA  
PROPYLENE GLYCOL  
METHYLPARABEN  
PROPYLPARABEN  
GLYCERYL MONOSTEARATE  
ISOPROPYL MYRISTATE  
CETOSTEARYL ALCOHOL  
SODIUM LAURYL SULFATE  
SODIUM CETOSTEARYL SULFATE  
POLYSORBATE 80  
CITRIC ACID MONOHYDRATE  
WATER  
Packaging
# Item Code Package Description
1 NDC:24730-802-04 118 g in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/02/2000
Labeler - United Pet Group (931135730)
Establishment
Name Address ID/FEI Operations
JUNGLE LABORATORIES CORPORATION 032615270 manufacture
Revised: 04/2010
 
United Pet Group



Hide