FDA Label for Lanoguard Dry Skin Therapy
View Indications, Usage & Precautions
Lanoguard Dry Skin Therapy Product Label
The following document was submitted to the FDA by the labeler of this product Summit Industries, Inc.. 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 37%
Purpose
Skin Protectant
Uses
- Helps protect ulcer prone skin.
- For treatment of cracked skin, minor burns or irritation.
- Helps prevent chafing and dryness.
Warnings
- For external use only.
- Avoid contact with eyes.
- Do not apply to deep or puncture wounds.
- If condition worsens, or does not improve within 7 days, consult a doctor.
- If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Keep Out Of Reach Of Children
- Keep out of reach of children.
Directions
- Gently cleanse and dry area.
- Massage liberally into affected area as needed.
- Cover treated feet.
Other Information
Store at 20-25°C (68-77°F)
Inactive Ingredients:
Beeswax (yellow wax), Fragrance, HEEDTA, Lanolin Alcohol, Mineral Oil, Oxyquinoline, Petrolatum, Purified Water, Sodium Borate, Sorbitan Sesquioleate
Questions Comments?
1-800-241-6996 or www.lantiseptic.com
SUMMIT INDUSTRIES, INC
Lantiseptic Division
PO BOX 7329
Marietta, GA 30065
Image Of Representative Artwork
LanoGuardDrySkinfouroz.jpg
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