Dosage & Administration
Clean the affected area. Apply Xcellderma. Reapply after 24 hours.
Xcellderma Cream
FDA Label NDC 84076-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Regenerex Pharma Inc for the product Xcellderma (NDC 84076-111). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding dosage & administration, warnings, indications & usage, inactive ingredient, otc - keep out of reach of children, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
Warnings: External use only. Avoid contact with eyes. Not to be applied over deep or puncture wounds, infections or lacerations. If condition worsens or does not improve within 7 days, stop use and consult a doctor.
Indications & Usage
Indications: To cover and protect abrasions, skin tears, pressure ulcers and minor burns.
Inactive Ingredient
Inactive ingredients: Polyethylene Glycol 4000, Polyethylene Glycol 400, Water, Citric Acid, Potassium Citrate, Benzoic Acid, Rubidium Chloride, Calcium Chloride.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
To serve as a wound protectant
Package Label.Principal Display Panel
Xcellderma Liquid Bandage/skin Protectant (Xcelld)
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