Hydrophor Ointment
FDA Label NDC 71399-5101

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Akron Pharma Inc. for the product Hydrophor (NDC 71399-5101). 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 drug facts, uses, warnings, indications & usage, otc - keep out of reach of children, directions, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient:

Petrolatum 42%

Purpose:

Skin protectant

Uses

  • Helps prevent and protects chafed, chapped or cracked skin.
  • Helps prevent and protect from the drying effects of wind and cold weather.

Warnings

For External Use Only.


Indications & Usage

When using this product:
  • Avoid contact with eyes.
  • If the condition worsens, discontinue use and contact a physician.

Otc - Keep Out Of Reach Of Children

  • KEEP OUT OF REACH OF CHILDREN.

Directions

  • Apply generously to affected areas or as directed by your physician.

Inactive Ingredient

Ceresin Wax, Lanolin, Mineral Oil, Paraffin Wax & Phenoxyethanol.

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