NDC 72186-012

Retreat

Calcium Fluoride, Calcium Phosphate, Unspecified Form, Calcium Sulfate, Unspecified Form, Ferrous Phosphate, Magnesium Phosphate, Tribasic, Pentahydrate, Potassium Chloride, Dibasic Potassium Phosphate, Sodium Chloride, Sodium Phosphate, Sodium Sulfate, Hydrated Silica, And Centaurea Benedicta

Retreat is a Sublingual Liquid in the Human Otc Drug category. It is labeled and distributed by Key Origins, Inc.. The primary component is Calcium Fluoride; Calcium Phosphate, Unspecified Form; Calcium Sulfate, Unspecified Form; Ferrous Phosphate; Magnesium Phosphate, Tribasic, Pentahydrate; Potassium Chloride; Dibasic Potassium Phosphate; Sodium Chloride; Sodium Phosphate; Sodium Sulfate; Hydrated Silica; Centaurea Benedicta.

• Product ID: 72186-012_37919c73-5a56-4168-80b8-3cdb4367f638
• NDC: 72186-012
• Product Type: Human Otc Drug
• Proprietary Name: Retreat
• Generic Name: Calcium Fluoride, Calcium Phosphate, Unspecified Form, Calcium Sulfate, Unspecified Form, Ferrous Phosphate, Magnesium Phosphate, Tribasic, Pentahydrate, Potassium Chloride, Dibasic Potassium Phosphate, Sodium Chloride, Sodium Phosphate, Sodium Sulfate, Hydrated Silica, And Centaurea Benedicta
• Dosage Form: Liquid
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2019-12-02
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Key Origins, Inc.
• Substance Name: CALCIUM FLUORIDE; CALCIUM PHOSPHATE, UNSPECIFIED FORM; CALCIUM SULFATE, UNSPECIFIED FORM; FERROUS PHOSPHATE; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; POTASSIUM CHLORIDE; DIBASIC POTASSIUM PHOSPHATE; SODIUM CHLORIDE; SODIUM PHOSPHATE; SODIUM SULFATE; HYDRATED SILICA; CENTAUREA BENEDICTA
• Active Ingredient Strength: 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72186-012-12

60 mL in 1 BOTTLE, SPRAY (72186-012-12)

• Marketing Start Date: 2019-12-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72186-012-12 [72186001212]

Retreat LIQUID

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-12-02

Drug Details

Active Ingredients

Ingredient	Strength
CALCIUM FLUORIDE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 42b1fc7d-dd7b-4251-9cc5-0abdcad97106
• Manufacturer:
  • Key Origins, Inc.
• UNII:
  • CI71S98N1Z
  • O3B55K4YKI
  • 6L5ZL09795
  • WAT0DDB505
  • 97Z1WI3NDX
  • 451W47IQ8X
  • 0YPR65R21J
  • Y6O7T4G8P9
  • D07L04MRWI
  • SE337SVY37
  • 453COF7817
  • 660YQ98I10
• UPC Code:
  • 0682157988020

NDC Crossover Matching brand name "Retreat" or generic name "Calcium Fluoride, Calcium Phosphate, Unspecified Form, Calcium Sulfate, Unspecified Form, Ferrous Phosphate, Magnesium Phosphate, Tribasic, Pentahydrate, Potassium Chloride, Dibasic Potassium Phosphate, Sodium Chloride, Sodium Phosphate, Sodium Sulfate, Hydrated Silica, And Centaurea Benedicta"

NDC	Brand Name	Generic Name
72186-011	Retreat	CALCIUM FLUORIDE, CALCIUM PHOSPHATE, UNSPECIFIED FORM, CALCIUM SULFATE, UNSPECIFIED FORM, FERROUS PHOSPHATE, MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE, POTASSIUM CHLORIDE, DIBASIC POTASSIUM PHOSPHATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, SODIUM SULFATE, HYDRATED SILICA, and CENTAUREA BENEDICTA
72186-012	Retreat	CALCIUM FLUORIDE, CALCIUM PHOSPHATE, UNSPECIFIED FORM, CALCIUM SULFATE, UNSPECIFIED FORM, FERROUS PHOSPHATE, MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE, POTASSIUM CHLORIDE, DIBASIC POTASSIUM PHOSPHATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, SODIUM SULFATE, HYDRATED SILICA, and CENTAUREA BENEDICTA