Label: APOMORPHINUM MURIATICUM- apomorphine hydrochloride pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 10191-1225-2 - Packager: Remedy Makers
- Category: HUMAN PRESCRIPTION DRUG LABEL
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 30, 2009
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- Official Label (Printer Friendly)
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INDICATIONS & USAGE
Free from yeast, wheat, corn, and soy.
DIRECTIONS: Dissolve 3 or 4 pellets
in mouth or under tongue 3 times a day or as directed by a physician.
Children 2 years and older take 1/2
adult dose.
INDICATIONS: To be used according
to standard homeopathic indications
for self limiting conditions such as
those indicated on the front panel or as directed by a physician.
Warnings: *Use only if cap and
seal are unbroken. * Keep this and all medications out of reach of children.
* If symptoms persist for more then 3
days, consult your physician.
*As with any drug, if your are pregnant or nursing a baby, seek the advice of a
health professional before using this product.*Store tightly closed in a cool, dark place.
Made according to The Homoeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
APOMORPHINUM MURIATICUM
apomorphine hydrochloride pelletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10191-1225 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APOMORPHINE HYDROCHLORIDE (UNII: F39049Y068) (APOMORPHINE - UNII:N21FAR7B4S) APOMORPHINE HYDROCHLORIDE 3 [hp_X] Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10191-1225-2 153 in 1 VIAL, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/18/2002 Labeler - Remedy Makers (018543582)
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