Label: DR. RECKEWEG R13 PROHAEMORRHIN COMBINATION PRODUCT- aesculus hippocastanum 2x, collinsonia canadensis 4x, graphites 8x, hamamelis virginiana 3x, kali carbonicum 6x, lycopodium clavatum 5x, nitricum acidum 6x, nux vomica 4x, paeonia officinalis 3x, sulphur 5x liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53346-1313-5 - 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 R13 PROHAEMORRHIN COMBINATION PRODUCT
aesculus hippocastanum 2x, collinsonia canadensis 4x, graphites 8x, hamamelis virginiana 3x, kali carbonicum 6x, lycopodium clavatum 5x, nitricum acidum 6x, nux vomica 4x, paeonia officinalis 3x, sulphur 5x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53346-1313 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HORSE CHESTNUT (UNII: 3C18L6RJAZ) (HORSE CHESTNUT - UNII:3C18L6RJAZ) HORSE CHESTNUT 2 [hp_X] in 50 mL COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (COLLINSONIA CANADENSIS ROOT - UNII:O2630F3XDR) COLLINSONIA CANADENSIS ROOT 4 [hp_X] in 50 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 8 [hp_X] in 50 mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 3 [hp_X] in 50 mL POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 6 [hp_X] in 50 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 5 [hp_X] in 50 mL NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID 6 [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 PAEONIA OFFICINALIS ROOT (UNII: 8R564U2E1P) (PAEONIA OFFICINALIS ROOT - UNII:8R564U2E1P) PAEONIA OFFICINALIS ROOT 3 [hp_X] in 50 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 5 [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:53346-1313-5 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(53346-1313)