Active Ingredient
Aluminum Hydroxide Gel 2%
Dermamed
FDA Label NDC 61924-214
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dermarite Industries, Llc for the product Dermamed (NDC 61924-214). 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 active ingredient, purpose, uses, warnings, directions, other information, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin protectant
Uses
Dries the oozing and weeping of poison: ivy, oak, or sumac, or other skin irritations.
Warnings
For external use only.
Avoid contact with eyes. In case of contact, flush thoroughly with water.
Stop and ask a doctor if
- condition worsens
- symptoms last more than 7 days or clear up and occur again within a few days
Keep out of reach of children.
In case of accidental ingestion contact a Physician or Poison Control Center right away.
Directions
Apply liberally to the affected area as needed or as directed by a physician.
Other Information
- Store at room temperature (59°- 86°F)
- You may report a serious adverse event to DermaRite Industries, PO Box 7209, North Bergen, NJ 07047.
Inactive Ingredients
Petrolatum, Lanolin, Water, Propylene Glycol, Stearyl Alcohol, Calcium Carbonate, Magnesium Hydroxide, Zinc Chloride, DMDM Hydantoin, Methylparaben, Propylparaben, Sodium Laureth Sulfate, Lanolin Alcohol, Cholecalciferol, Zea Mays (Corn) Oil, Retinyl Palmitate, Citric Acid, Sodium Chloride
Questions?
Call 800-337-6296 Mon - Fri 9AM - 5PM EST.
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