Ammonium Lactate: Topical lotion (12%)
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What is this Medicine?
AMMONIUM LACTATE (uh MOH nee uhm LAK teyt) is used on the skin to treat dry skin and other skin conditions.
Ammonium Lactate 12% Topical Lotion
NDC: 458020419-
Prescription Required
-
Not a Controlled Drug
(CSA Schedule) -
FDA Approved
Xerosis, Ichthyosis
Store at room temperature (between 59 to 86 degrees F)
Reported Side Effects for Ammonium Lactate 12% Topical Lotion
Onset: DELAYED
Onset: EARLY
Onset: RAPID
Onset: EARLY
Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.
Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.
Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.
Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.
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