Lanoguard
FDA Label NDC 12090-0042

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Summit Industries, Inc. for the product Lanoguard (NDC 12090-0042). 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, otc - keep out of reach of children, 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

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

Label (Lanoguarddryskinfouroz)

Label (Lanoguarddryskinfouroz)

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