Label: BIOCHEMIC PHOSPHATE- tribasic calcium phosphate, ferrosoferric phosphate, potassium phosphate, dibasic, magnesium phosphate, dibasic trihydrate, and sodium phosphate, dibasic, heptahydrate tablet
- NDC Code(s): 54973-1069-1, 54973-1069-2
- Packager: Hyland's 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 November 29, 2022
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INGREDIENTS AND APPEARANCE
BIOCHEMIC PHOSPHATE
tribasic calcium phosphate, ferrosoferric phosphate, potassium phosphate, dibasic, magnesium phosphate, dibasic trihydrate, and sodium phosphate, dibasic, heptahydrate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-1069 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (PHOSPHATE ION - UNII:NK08V8K8HR) TRIBASIC CALCIUM PHOSPHATE 3 [hp_X] FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 3 [hp_X] POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) POTASSIUM PHOSPHATE, DIBASIC 3 [hp_X] MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 3 [hp_X] SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR, SODIUM CATION - UNII:LYR4M0NH37) SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 3 [hp_X] Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-1069-1 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/19/1979 12/27/2021 2 NDC:54973-1069-2 1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/19/1979 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/19/1979 Labeler - Hyland's Inc. (008316655) Establishment Name Address ID/FEI Business Operations Hyland's Inc. 008316655 manufacture(54973-1069) , pack(54973-1069)