Label: ELECTROLYTE PLUS- boron citrate, calcium gluconate, chromium picolinate, cobalt gluconate, copper gluconate, ferrous muriaticum, magnesium gluconicum dihydricum, manganese gluconate, potassium gluconate, selenium dioxide, sodium gluconate, zincum gluconicum, kali phosphoricum, niccolum metallicum, vanadium metallicum, calcarea phosphorica liquid
- NDC Code(s): 43742-1516-1
- Packager: Deseret Biologicals, 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 October 11, 2023
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ACTIVE INGREDIENTS:
Boron Citrate 6X, Calcium Gluconate 6X, Chromium Picolinate 6X, Cobalt Gluconate 6X, Copper Gluconate 6X, Ferrous Muriaticum 6X, Magnesium Gluconicum Dihydricum 6X, Manganese Gluconate 6X, Potassium Gluconate 6X, Selenium Dioxide 6X, Sodium Gluconate 6X, Zincum Gluconicum 6X, Kali Phosphoricum 8X, Niccolum Metallicum 8X, Vanadium Metallicum 8X, Calcarea Phosphorica 9X.
- HOMEOPATHIC INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- HOMEOPATHIC INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
ELECTROLYTE PLUS
boron citrate, calcium gluconate, chromium picolinate, cobalt gluconate, copper gluconate, ferrous muriaticum, magnesium gluconicum dihydricum, manganese gluconate, potassium gluconate, selenium dioxide, sodium gluconate, zincum gluconicum, kali phosphoricum, niccolum metallicum, vanadium metallicum, calcarea phosphorica liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-1516 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BORON CITRATE (UNII: S043P4DV22) (BORON - UNII:N9E3X5056Q) BORON CITRATE 6 [hp_X] in 1 mL CALCIUM GLUCONATE (UNII: SQE6VB453K) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM GLUCONATE 6 [hp_X] in 1 mL CHROMIUM PICOLINATE (UNII: S71T8B8Z6P) (CHROMIC CATION - UNII:X1N4508KF1) CHROMIC CATION 6 [hp_X] in 1 mL COBALTOUS GLUCONATE (UNII: 26SK597UWV) (COBALTOUS CATION - UNII:AI1MR454XG) COBALTOUS GLUCONATE 6 [hp_X] in 1 mL COPPER GLUCONATE (UNII: RV823G6G67) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC CATION 6 [hp_X] in 1 mL FERRIC CHLORIDE HEXAHYDRATE (UNII: 0I2XIN602U) (FERRIC CATION - UNII:91O4LML611) FERRIC CATION 6 [hp_X] in 1 mL MAGNESIUM GLUCONATE (UNII: T42NAD2KHC) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM GLUCONATE 6 [hp_X] in 1 mL MANGANESE GLUCONATE (UNII: 9YY2F980SV) (MANGANESE CATION (2+) - UNII:H6EP7W5457) MANGANESE GLUCONATE 6 [hp_X] in 1 mL POTASSIUM GLUCONATE (UNII: 12H3K5QKN9) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM GLUCONATE 6 [hp_X] in 1 mL SELENIUM DIOXIDE (UNII: 9N3UK29E57) (SELENIUM DIOXIDE - UNII:9N3UK29E57) SELENIUM DIOXIDE 6 [hp_X] in 1 mL SODIUM GLUCONATE (UNII: R6Q3791S76) (GLUCONIC ACID - UNII:R4R8J0Q44B) SODIUM GLUCONATE 6 [hp_X] in 1 mL ZINC GLUCONATE (UNII: U6WSN5SQ1Z) (ZINC CATION - UNII:13S1S8SF37) ZINC GLUCONATE 6 [hp_X] in 1 mL DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) DIBASIC POTASSIUM PHOSPHATE 8 [hp_X] in 1 mL NICKEL (UNII: 7OV03QG267) (NICKEL - UNII:7OV03QG267) NICKEL 8 [hp_X] in 1 mL VANADIUM (UNII: 00J9J9XKDE) (VANADIUM - UNII:00J9J9XKDE) VANADIUM 8 [hp_X] in 1 mL TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 9 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) DEXTROSE MONOHYDRATE (UNII: LX22YL083G) ALCOHOL (UNII: 3K9958V90M) ARGININE (UNII: 94ZLA3W45F) LEVOCARNITINE (UNII: 0G389FZZ9M) LEUCINE (UNII: GMW67QNF9C) ORNITHINE (UNII: E524N2IXA3) VALINE (UNII: HG18B9YRS7) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) GRAPE (UNII: 6X543N684K) POTASSIUM CHLORIDE (UNII: 660YQ98I10) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-1516-1 120 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/21/2019 03/16/2027 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/21/2019 03/16/2027 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-1516) , api manufacture(43742-1516) , label(43742-1516) , pack(43742-1516)