Label: FIBRO RELIEF- ferrum metallicum, guaiacum, lithium carbonicum, lycopersicum esculentum, magnesia phosphorica capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 57520-0272-1 - Packager: Apotheca Company
- 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 20, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FIBRO RELIEF
ferrum metallicum, guaiacum, lithium carbonicum, lycopersicum esculentum, magnesia phosphorica capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0272 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON 30 [hp_C] GUAIACUM OFFICINALE RESIN (UNII: N0K2Z502R6) (GUAIACUM OFFICINALE RESIN - UNII:N0K2Z502R6) GUAIACUM OFFICINALE RESIN 30 [hp_C] LITHIUM CARBONATE (UNII: 2BMD2GNA4V) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM CARBONATE 30 [hp_C] TOMATO (UNII: Z4KHF2C175) (TOMATO - UNII:Z4KHF2C175) TOMATO 30 [hp_C] MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 30 [hp_C] Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) NYMPHAEA ODORATA ROOT (UNII: 69RAZ4C432) POWDERED CELLULOSE (UNII: SMD1X3XO9M) MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA) ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) EUROPEAN ELDERBERRY (UNII: BQY1UBX046) LOBELIA INFLATA (UNII: 9PP1T3TC5U) RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) Product Characteristics Color white (Clear) Score no score Shape CAPSULE (NONE) Size 25mm Flavor Imprint Code NONE Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57520-0272-1 120 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/17/2010 Labeler - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture