Label: CEDAR FEVER- onion - fraxinus americana bark - galphimia glauca flowering top - juniperus virginiana twig - quercus robur twig bark - thuja plicata leaf - ulmus rubra bark liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69406-002-11 - Packager: People's Pharmacy, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- 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 January 27, 2016
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- ACTIVE INGREDIENTS
- USES
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- INDICATIONS
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- INACTIVE INGREDIENTS
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INGREDIENTS AND APPEARANCE
CEDAR FEVER
onion - fraxinus americana bark - galphimia glauca flowering top - juniperus virginiana twig - quercus robur twig bark - thuja plicata leaf - ulmus rubra bark liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69406-002 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 6 [hp_X] in 30 mL FRAXINUS AMERICANA BARK (UNII: 0B24UR1O1S) (FRAXINUS AMERICANA BARK - UNII:0B24UR1O1S) FRAXINUS AMERICANA BARK 6 [hp_X] in 30 mL GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E) GALPHIMIA GLAUCA FLOWERING TOP 6 [hp_X] in 30 mL JUNIPERUS VIRGINIANA TWIG (UNII: 532BCG080L) (JUNIPERUS VIRGINIANA TWIG - UNII:532BCG080L) JUNIPERUS VIRGINIANA TWIG 6 [hp_X] in 30 mL QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947) (QUERCUS ROBUR TWIG BARK - UNII:2JFK226947) QUERCUS ROBUR TWIG BARK 6 [hp_X] in 30 mL THUJA PLICATA LEAF (UNII: R9I752FESH) (THUJA PLICATA LEAF - UNII:R9I752FESH) THUJA PLICATA LEAF 6 [hp_X] in 30 mL ULMUS RUBRA BARK (UNII: 91QY4PXU8Q) (ULMUS RUBRA BARK - UNII:91QY4PXU8Q) ULMUS RUBRA BARK 6 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69406-002-11 30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/28/2015 Labeler - People's Pharmacy, Inc (051659639) Registrant - Washington Homeopathic Products (084929389) Establishment Name Address ID/FEI Business Operations Washington Homeopathic Products 084929389 manufacture(69406-002)
