Label: REYNOUTRIA LYME liquid
- NDC Code(s): 48951-8396-3
- Packager: Uriel 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 October 11, 2022
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
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ACTIVE INGREDIENT
Active Ingredients: Reynoutria japonica (Japanese knotweed) 3X, Dipsacus sylvestris (Teasel) 4X, Helleborus (Christmas rose) 4X,
Astragalus membranaceus e rad. (Milk vetch) 6X, Argentum (Silver) 17X, Cuprum (Copper) 17X, Quartz (Rock crystal) 17X, Apis (Honeybee) 21X, Astragalus membraceus e fol. et sem. (Milk vetch) 30X, Aurum (Metallic gold) 30X - INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
- QUESTIONS
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INGREDIENTS AND APPEARANCE
REYNOUTRIA LYME
reynoutria lyme liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8396 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 17 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 17 [hp_X] in 1 mL APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 21 [hp_X] in 1 mL ASTRAGALUS CHINENSIS SEED (UNII: U046B39ADE) (ASTRAGALUS CHINENSIS SEED - UNII:U046B39ADE) ASTRAGALUS CHINENSIS SEED 30 [hp_X] in 1 mL GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 30 [hp_X] in 1 mL SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 17 [hp_X] in 1 mL HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815) HELLEBORUS NIGER ROOT 4 [hp_X] in 1 mL DIPSACUS FULLONUM WHOLE (UNII: 1FT87R544S) (DIPSACUS FULLONUM WHOLE - UNII:1FT87R544S) DIPSACUS FULLONUM WHOLE 4 [hp_X] in 1 mL ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (ASTRAGALUS PROPINQUUS ROOT - UNII:922OP8YUPF) ASTRAGALUS PROPINQUUS ROOT 6 [hp_X] in 1 mL REYNOUTRIA JAPONICA LEAF (UNII: 2540B7G25G) (REYNOUTRIA JAPONICA LEAF - UNII:2540B7G25G) REYNOUTRIA JAPONICA LEAF 3 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-8396-3 60 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy, Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy, Inc 043471163 manufacture(48951-8396)
