LANOGUARD DRY SKIN THERAPY- lanolin cream

LanoGuard by

Drug Labeling and Warnings

LanoGuard by is a Otc medication manufactured, distributed, or labeled by Summit Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

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

INGREDIENTS AND APPEARANCE

LANOGUARD  DRY SKIN THERAPY
lanolin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12090-0042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H)	LANOLIN	370 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
YELLOW WAX (UNII: 2ZA36H0S2V)
HYDROXYETHYLETHYLENEDIAMINETRIACETIC ACID (UNII: R79J91U341)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
MINERAL OIL (UNII: T5L8T28FGP)
OXYQUINOLINE (UNII: 5UTX5635HP)
PETROLATUM (UNII: 4T6H12BN9U)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12090-0042-5	113 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	12/30/2009

Labeler - Summit Industries, Inc. (003279189)

Establishment
Name	Address	ID/FEI	Business Operations
Summit Industries, Inc.		003279189	manufacture(12090-0042)