Label: DR. RECKEWEG R65 PSORIASIN COMBINATION PRODUCT- berberis aquifolium 4x, hydrocotyle asiatica 4x, arsenicum album 12x, calcarea carbonica 30x, graphites 12x, natrum muriaticum 30x liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53346-1365-5 - 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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INGREDIENTS AND APPEARANCE
DR. RECKEWEG R65 PSORIASIN COMBINATION PRODUCT
berberis aquifolium 4x, hydrocotyle asiatica 4x, arsenicum album 12x, calcarea carbonica 30x, graphites 12x, natrum muriaticum 30x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53346-1365 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAHONIA AQUIFOLIUM WHOLE (UNII: J4WG1JVR05) (MAHONIA AQUIFOLIUM WHOLE - UNII:J4WG1JVR05) MAHONIA AQUIFOLIUM WHOLE 4 [hp_X] in 50 mL CENTELLA ASIATICA (UNII: 7M867G6T1U) (CENTELLA ASIATICA - UNII:7M867G6T1U) CENTELLA ASIATICA 4 [hp_X] in 50 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 12 [hp_X] in 50 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X] in 50 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 12 [hp_X] in 50 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 30 [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:53346-1365-5 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(53346-1365)