NDC 57955-0131

Calcium Metabolizer

Calcarea Acetica, Calcarea Carbonica, Calcarea Caustica, Calcarea Fluorica, Calcarea Iodata, Calcarea Lactica, Calcarea Muriatica, Calcarea Oxalica, Calcarea Phosphorica, Calcarea Silicata, Calcarea Sulphurica, Hekla Lava, Silicea

Calcium Metabolizer is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Calcium Acetate; Oyster Shell Calcium Carbonate, Crude; Calcium Hydroxide; Calcium Fluoride; Calcium Iodide; Calcium Lactate Pentahydrate; Calcium Chloride; Calcium Oxalate Monohydrate; Tribasic Calcium Phosphate; Calcium Silicate; Calcium Sulfate Anhydrous; Hekla Lava; Silicon Dioxide.

Product ID57955-0131_e8a85e53-2701-480e-a617-e456af964009
NDC57955-0131
Product TypeHuman Otc Drug
Proprietary NameCalcium Metabolizer
Generic NameCalcarea Acetica, Calcarea Carbonica, Calcarea Caustica, Calcarea Fluorica, Calcarea Iodata, Calcarea Lactica, Calcarea Muriatica, Calcarea Oxalica, Calcarea Phosphorica, Calcarea Silicata, Calcarea Sulphurica, Hekla Lava, Silicea
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-02-20
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameKing Bio Inc.
Substance NameCALCIUM ACETATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM HYDROXIDE; CALCIUM FLUORIDE; CALCIUM IODIDE; CALCIUM LACTATE PENTAHYDRATE; CALCIUM CHLORIDE; CALCIUM OXALATE MONOHYDRATE; TRIBASIC CALCIUM PHOSPHATE; CALCIUM SILICATE; CALCIUM SULFATE ANHYDROUS; HEKLA LAVA; SILICON DIOXIDE
Active Ingredient Strength10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 57955-0131-2

59 mL in 1 BOTTLE, SPRAY (57955-0131-2)
Marketing Start Date2015-02-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57955-0131-2 [57955013102]

Calcium Metabolizer LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-02-20
Inactivation Date2020-01-31

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.