Label: DR. RECKEWEG R11 LUMBAGIN COMBINATION PRODUCT- berberis vulgaris 4x, calcarea phosphorica 12x, causticum 6x, dulcamara 4x, nux vomica 4x, rhododendron chrysanthum 4x, rhus toxicodendron 4x liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53346-1311-5 - Packager: PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
- 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 April 3, 2013
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- ACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
DR. RECKEWEG R11 LUMBAGIN COMBINATION PRODUCT
berberis vulgaris 4x, calcarea phosphorica 12x, causticum 6x, dulcamara 4x, nux vomica 4x, rhododendron chrysanthum 4x, rhus toxicodendron 4x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53346-1311 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 CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP) (CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS - UNII:L11K75P92J) CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE 12 [hp_X] in 50 mL CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM 6 [hp_X] in 50 mL SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP 4 [hp_X] in 50 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 4 [hp_X] in 50 mL RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U) RHODODENDRON AUREUM LEAF 4 [hp_X] in 50 mL TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 4 [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:53346-1311-5 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(53346-1311)