Active Ingredient:
Petrolatum 44.28%
Tenderphor Ointment
FDA Label NDC 69771-014
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Geri-gentle Corporation for the product Tenderphor (NDC 69771-014). 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:, warnings:, directions:, other information:, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose:
Skin Protectant
Uses:
- Temporarily protects minor cuts, scrapes, burns.
- Temporarily protects and helps relieve chapped or cracked skin and lips.
- Helps protect skin from the drying effects of wind and cold weather.
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
Warnings:
Do not use on deep or puncture wounds, animal bites, or serious wounds.
Keep out of reach of children.
Incase of accidental ingestion contact a Physician or Poison Control Center right away.
Directions:
Apply liberally to affected area as needed.
Other Information:
■Store at room temperature 15°-30°C (68°-77°F)
Inactive Ingredients:
Lanolin Alcohol, Light Liquid Paraffin, Microcrystalline Wax, Paraffin
* Please review the disclaimer below.
