Label: MORPHINUM MURIATICUM- morphine hydrochloride pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 10191-1029-2 - Packager: Remedy Makers
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: CII
- Marketing Status: unapproved homeopathic
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 March 7, 2011
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- CONTROLLED SUBSTANCE
- INDICATIONS & USAGE
- WARNINGS
- INDICATIONS & USAGE
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WARNINGS
WARNING SECTION: Use only if cap and seal are unbroken. If symptoms persist for more than 3 days, contact your physician or pharmacist. Do not take if you are pregnant or nursing a baby. Store tightly closed in a cool, dark place. Made according to The Homeopathic Pharmacopoeia of the United State by: Remedy Makers, Pomona, CA 91768
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INGREDIENTS AND APPEARANCE
MORPHINUM MURIATICUM
morphine hydrochloride pelletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10191-1029 Route of Administration SUBLINGUAL DEA Schedule CII Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORPHINE HYDROCHLORIDE (UNII: J28GE0ROVX) (MORPHINE - UNII:76I7G6D29C) MORPHINE HYDROCHLORIDE 30 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10191-1029-2 130 in 1 VIAL, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/09/2002 Labeler - Remedy Makers (018543582)