Label: URINARY NOSODE COMBINATION 9410- urinary nosode combination liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-9410-1 - Packager: Professional Complementary Health Formulas
- 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 August 15, 2019
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WARNINGS
Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, rash, blood in urine, or persistent headache, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.
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INGREDIENTS AND APPEARANCE
URINARY NOSODE COMBINATION 9410
urinary nosode combination liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-9410 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TURPENTINE OIL (UNII: C5H0QJ6V7F) (TURPENTINE OIL - UNII:C5H0QJ6V7F) TURPENTINE OIL 4 [hp_X] in 29.5 mL ONONIS REPENS WHOLE (UNII: 7J37EHM6J6) (ONONIS REPENS WHOLE - UNII:7J37EHM6J6) ONONIS REPENS WHOLE 6 [hp_X] in 29.5 mL LYTTA VESICATORIA (UNII: 3Q034RO3BT) (LYTTA VESICATORIA - UNII:3Q034RO3BT) LYTTA VESICATORIA 8 [hp_X] in 29.5 mL BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 10 [hp_X] in 29.5 mL PROTEUS MORGANII (UNII: 56X6LID5ZY) (PROTEUS MORGANII - UNII:56X6LID5ZY) PROTEUS MORGANII 12 [hp_X] in 29.5 mL LEPTOSPIRA INTERROGANS (UNII: 84X67520MF) (LEPTOSPIRA INTERROGANS - UNII:84X67520MF) LEPTOSPIRA INTERROGANS 12 [hp_X] in 29.5 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63083-9410-1 29.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-9410)