FDA Label for Lantiseptic Dry Skin Therapy
View Indications, Usage & Precautions
Lantiseptic Dry Skin Therapy Product Label
The following document was submitted to the FDA by the labeler of this product Dermarite Industries Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Lanolin USP 30%
Purpose
Skin Protectant
Uses
- Temporarily protects minor cuts, scrapes, and burns
- Helps prevent and temporarily protects chafed, chapped, or cracked skin.
Warnings
• For external use only. • Avoid contact with eyes. •In case of contact, flush thoroughly with water.
Do not use on
- deep or puncture wounds
- animal bites
- serious burns
- conditions worsen
- symptoms last more than 7 days or clear up and occur again within a few days.
Stop use and ask a doctor if
Keep our of reach of children
In case of accidental ingestion contact a physician or Poison Control Center right away.
Directions
Apply liberally to affected area as needed or as directed by a physician.
Other Information
- Store at room temperature (59-86°F)
- You may report a serious adverse event to DermaRite Industries, PO Box 7209, North Bergen, NJ07047
Inactive Ingredients
Water, Mineral Oil, Petrolatum, Cera Alba, Sodium Borate, DMDM Hydantoin, Sorbitan Sesquioleate, Lanolin Alcohol, Disodium EDTA
Questions Or Comments?
Call 1-800-337-6296 Mon-Fri 9AM-5PM EST.
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