FDA records indicate that there are no current recalls for this drug.
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Questions & Answers
Side Effects & Adverse Reactions
Sun exposure to areas of the skin treated with LAClotion™ should be minimized or avoided (see PRECAUTIONS section). The use of LAClotion™ should be discontinued if any hypersensitivity is observed.
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
LAClotion™ (ammonium lactate) is indicated for the treatment of dry, scaly skin (xerosis) and ichthyosis vulgaris and for temporary relief of itching associated with these conditions.
History
There is currently no drug history available for this drug.
Other Information
LAClotion™ (ammonium lactate) specially formulates 12% lactic acid, neutralized with ammonium hydroxide, as ammonium lactate to provide a lotion pH of 4.5-5.5. LAClotion™ also contains light mineral oil, glyceryl stearate, PEG-100 stearate, propylene glycol, polyoxyl 40 stearate, glycerin, magnesium aluminum silicate, laureth-4, cetyl alcohol, methylcellulose, methyl and propyl parabens, and water. Lactic acid is a racemic mixture of 2-hydroxypropanoic acid and has the following structural formula:
Sources
Laclotion Manufacturers
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Paddock Laboratories, Inc.
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