Dosage
Active Ingredient Purpose
Zinc Oxide 20% w/w .
Zinc Oxide Pharma Ointment
FDA Label NDC 84387-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Allied Trade Link Llc for the product Zinc Oxide Pharma (NDC 84387-001). 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, warnings, inactive, indications & usage, otc - keep out of reach of children, otc - purpose, oxide zinc, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
For External Use Only
When using this product Do not get into eyes Do not use over large areas of the body
Stop use and ask a doctor if The condition worsens Symptoms last more than 7 days or clear up and occur again within a few days You are allergic to any of these
ingredients
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Inactive
Inactive Ingredients
Cetostearyl Alcohol, Light Mineral Oil, Macrogol Cetostearyl Ether 20, White Petrolatum
Indications & Usage
Directions
For poison ivy, oak, and sumac: apply as needed.
Uses
Dries the oozing and weeping of poison: Ivy Oak Sumac
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Otc - Purpose
PURPOSE SINK PROTECTANT
Oxide Zinc
Oxide (Oxide)
* Please review the disclaimer below.
