Label: DR. RECKEWEG R18 CYSTOPHYLIN COMBINATION PRODUCT- berberis vulgaris 4x, cantharis 4x, dulcamara 4x, equisetum hyemale 6x, eupatorium purpureum 3x liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53346-1318-5 - Packager: PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
- Category: HUMAN OTC DRUG LABEL
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 April 4, 2013
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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PRINCIPAL DISPLAY PANEL
NDC# 53346-1318-5
Dr. Reckeweg R18 Cystophylin
Homeopathic preparation for the temporary relief of minor symptoms associated with bladder infection such as:
- Minor urinary discomfort
- Pain and burning upon urination
- Feeling or urinary urgency
Manufactured by:
Dr. Reckeweg Co. GmbH
D-64625 Bensheim
Germany
1.68 fl oz
(50 ml) -
INGREDIENTS AND APPEARANCE
DR. RECKEWEG R18 CYSTOPHYLIN COMBINATION PRODUCT
berberis vulgaris 4x, cantharis 4x, dulcamara 4x, equisetum hyemale 6x, eupatorium purpureum 3x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53346-1318 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 4 [hp_X] in 50 mL LYTTA VESICATORIA (UNII: 3Q034RO3BT) (LYTTA VESICATORIA - UNII:3Q034RO3BT) LYTTA VESICATORIA 4 [hp_X] in 50 mL SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP 4 [hp_X] in 50 mL EQUISETUM HYEMALE (UNII: 59677RXH25) (EQUISETUM HYEMALE - UNII:59677RXH25) EQUISETUM HYEMALE 6 [hp_X] in 50 mL EUTROCHIUM PURPUREUM ROOT (UNII: 0VYG5PVN5Q) (EUTROCHIUM PURPUREUM ROOT - UNII:0VYG5PVN5Q) EUTROCHIUM PURPUREUM ROOT 3 [hp_X] in 50 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:53346-1318-5 50 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/01/1986 Labeler - PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO (318602612) Establishment Name Address ID/FEI Business Operations PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO 318602612 manufacture(53346-1318)