Label: BIO-COMBINATION 28- calcarea fluorica, calcarea phosphorica, calcarea sulphurica, ferrum phosphoricum, kali muriaticum, kali phosphoricum,kali sulphuricum, magnesia phosphorica, natrum muriaticum, natrum phosphoricum, natrum sulphuricum, silicea tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 15631-2383-0, 15631-2383-1, 15631-2383-2, 15631-2383-3, view more15631-2383-4, 15631-2383-5, 15631-2383-6, 15631-2383-7 - Packager: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
- 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 4, 2016
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ACTIVE INGREDIENT
CALCAREA FLUORICA 3X HPUS, CALCAREA PHOSPHORICA 3X HPUS, CALCAREA SULPHURICA 3X HPUS, FERRUM PHOSPHORICUM 3X HPUS, KALI MURIATICUM 3X HPUS, KALI PHOSPHORICUM 3X HPUS, KALI SULPHURICUM 3X HPUS, MAGNESIA PHOSPHORICA 3X HPUS, NATRUM MURIATICUM 3X HPUS, NATRUM PHOSPHORICUM 3X HPUS, NATRUM SULPHURICUM 3X HPUS, SILICEA 3X HPUS
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QUESTIONS OR COMMENTS
www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com
Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758
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INGREDIENTS AND APPEARANCE
BIO-COMBINATION 28
calcarea fluorica, calcarea phosphorica, calcarea sulphurica, ferrum phosphoricum, kali muriaticum, kali phosphoricum,kali sulphuricum, magnesia phosphorica, natrum muriaticum, natrum phosphoricum, natrum sulphuricum, silicea tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15631-2383 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 3 [hp_X] TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 3 [hp_X] CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 3 [hp_X] FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 3 [hp_X] POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 3 [hp_X] POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) POTASSIUM PHOSPHATE, DIBASIC 3 [hp_X] POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 3 [hp_X] MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 3 [hp_X] SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 3 [hp_X] SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 3 [hp_X] SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 3 [hp_X] SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 3 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15631-2383-0 1 in 1 BLISTER PACK; Type 6: Drug/Biologic Combination 04/04/2016 2 NDC:15631-2383-1 4 in 1 BLISTER PACK; Type 6: Drug/Biologic Combination 04/04/2016 3 NDC:15631-2383-2 50 in 1 CONTAINER; Type 6: Drug/Biologic Combination 04/04/2016 4 NDC:15631-2383-3 100 in 1 CONTAINER; Type 6: Drug/Biologic Combination 04/04/2016 5 NDC:15631-2383-4 250 in 1 CONTAINER; Type 6: Drug/Biologic Combination 04/04/2016 6 NDC:15631-2383-5 500 in 1 CONTAINER; Type 6: Drug/Biologic Combination 04/04/2016 7 NDC:15631-2383-6 1000 in 1 CONTAINER; Type 6: Drug/Biologic Combination 04/04/2016 8 NDC:15631-2383-7 10000 in 1 CONTAINER; Type 6: Drug/Biologic Combination 04/04/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/04/2016 Labeler - Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994) Establishment Name Address ID/FEI Business Operations Rxhomeo, Inc 832534981 wholesale drug distributor(15631-2383) Establishment Name Address ID/FEI Business Operations Rxhomeo Private Limited d.b.a. Rxhomeo, Inc 650833994 manufacture(15631-2383) , label(15631-2383)