Supraderm Cream
FDA Label NDC 52358-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Olen Skin Care Corporation for the product Supraderm (NDC 52358-0002). 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, active ingredients, purpose, use, warnings, otc - when using, otc - ask doctor, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
White Petrolatum 30%
Lanolin 15%
Purpose
Skin Protectant
Skin Protectant
Use
Temporarily Protects Minor:
- Cuts
- Scrapes
- Burns
- Temporarily protects and helps relieve chapped or cracked skin
- Helps protect from the drying effects of wind and cold weather
Warnings
For External Use Only
Otc - When Using
- Do not get into eyes
Otc - Ask Doctor
Stop use and ask a doctor if
- Condition worsens
- Symptoms last more that 7 days or clear up and occur again within a few days
Otc - Do Not Use
Do not use on
- Deep or puncture wounds
- Animal bites
- Serious burns
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children. If swallowed, get medical help or contact a Poison control Center right away.
Directions
Apply liberally to affected area of the skin as needed.
Other Information
Store between 59-86°F
Inactive Ingredients
zinc oxide, corn starch
Questions?
1-877-494-4313
Principal Display Panel
SUPRADERM
Skin Protectant
Barrier & Healing Cream
100% Natural
Hypoallergenic
* Please review the disclaimer below.
