FDA Label for Veradex-e
View Indications, Usage & Precautions
Veradex-e Product Label
The following document was submitted to the FDA by the labeler of this product Abbe Laboratories, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredients
Petrolatum USP 58.95%
Anhydrous Lanolin USP 35%
Otc - Purpose
Purpose
Petrolatum USP 58.95% .................................. Protectant
Anhydrous Lanolin USP 35% ....................... Protectant
Inactive Ingredient
Other ingredients: Tocopheryl Acetate, Cetyl Esters, Ethyl Methylphenylglycidate, Benzyl Cinnamate, Salicylic Acid.
Warnings
Warnings: For external use only.
Discontinue use if signs of irritation appear. If condition worsens consult a doctor.
Do not use over deep, infected, or puncture wounds.
Otc - Keep Out Of Reach Of Children
Keep from children.
Indications & Usage
Indications: Temporarily relieves minor burns, dry, chapped, fissured and macerated skin and lips, also relieves Psoriais, Eczema, mild sunburn, abrasions and contusions, diaper dermatitis, hemorrhoids, and prickly heat.
Dosage & Administration
Directions: Apply a thin film to clean, dry skin three times daily. May be covered with sterile gauze, if desired.
Package Label.Principal Display Panel
NDC 68605-3700-5
VERADEX-E® OINTMENT
Super Emollient, Protectant
Healing Ointment
Net Wt. 100g.
U.S. Pat. # 5,645,826
ABBE LABORATORIES, INC.TM
Farmingdale, NY 11735
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