Active Ingredient
Aluminum Hydroxide Gel 2%
Procure Drydrox Ointment
FDA Label NDC 55681-031
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Twin Med Llc for the product Procure Drydrox (NDC 55681-031). 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, directions, inactive ingredients, warnings, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin Protectant
Uses
Uses
- Dries the oozing and weeping of poison ivy, oak and sumac
Directions
Directions
- Apply as needed
- Children under 6 months of age: ask a doctor
Inactive Ingredients
Calcium Carbonate, Cholecalciferol, Citric Acid, Ethylhexylglycerin, Glyceryl Monostearate, Glyceryl Stearate/ PEG-100 Stearate, Lanolin, Magnesium Hydroxide, Petrolatum, Phenoxyethanol, Propylene Glycol, Retinyl Palmitate, Sodium Chloride, Sodium Laureth Sulfate,Stearyl Alcohol, Water, Zea Mays Corn Oil, Zinc Chloride
Warnings
Warnings
For external use only
When Using This Product
When using this productdo not get into the eyes
Stop Use And Ask A Doctor If
Stop use 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
Keep out of reach of children.In case of accidental ingestion contact a physician or Poison Control Center right away.
* Please review the disclaimer below.
