Label: CHLORALUM- chloral hydrate pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 10191-1177-2 - Packager: Remedy Makers
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: CIV
- 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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
WARNING: Used only if cap and seal are unbroken. If symptoms persist for more then 3 days, consult your physician. As with any drug, if your pregnant or nursing a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool, dark place. Made according to The Homeopathic Pharmacopoeia of the United State by: Remedy Makers, Pomona, CA 91768.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CHLORALUM
chloral hydrate pelletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10191-1177 Route of Administration SUBLINGUAL DEA Schedule CIV Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORAL HYDRATE (UNII: 418M5916WG) (CHLORAL - UNII:FLI06WS32H) CHLORAL HYDRATE 3 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10191-1177-2 172 in 1 VIAL, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/04/2000 Labeler - Remedy Makers (018543582)
