Label: 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 gel
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 liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72186-011-11, 72186-012-12 - Packager: Key Origins, Inc.
- Category: HUMAN OTC DRUG LABEL
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 December 26, 2019
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Ingredients
- SPL UNCLASSIFIED SECTION
- WARNINGS
- SPL UNCLASSIFIED SECTION
- Descriptions
- Directions
- SPL UNCLASSIFIED SECTION
- Ingredients
- SPL UNCLASSIFIED SECTION
- WARNINGS
- SPL UNCLASSIFIED SECTION
- Descriptions
- Directions
- PRINCIPAL DISPLAY PANEL - 1 oz Jar Label
- PRINCIPAL DISPLAY PANEL - 2 oz Bottle Spray
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INGREDIENTS AND APPEARANCE
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 gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72186-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 6 [hp_X] in 1 mL CALCIUM PHOSPHATE, UNSPECIFIED FORM (UNII: 97Z1WI3NDX) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM PHOSPHATE, UNSPECIFIED FORM 6 [hp_X] in 1 mL CALCIUM SULFATE, UNSPECIFIED FORM (UNII: WAT0DDB505) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE, UNSPECIFIED FORM 6 [hp_X] in 1 mL FERROUS PHOSPHATE (UNII: D07L04MRWI) (FERROUS CATION - UNII:GW89581OWR) FERROUS PHOSPHATE 6 [hp_X] in 1 mL MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE (UNII: 453COF7817) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE 6 [hp_X] in 1 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 6 [hp_X] in 1 mL DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR, POTASSIUM CATION - UNII:295O53K152) DIBASIC POTASSIUM PHOSPHATE 6 [hp_X] in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 6 [hp_X] in 1 mL SODIUM PHOSPHATE (UNII: SE337SVY37) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE 6 [hp_X] in 1 mL SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 6 [hp_X] in 1 mL HYDRATED SILICA (UNII: Y6O7T4G8P9) (HYDRATED SILICA - UNII:Y6O7T4G8P9) HYDRATED SILICA 6 [hp_X] in 1 mL CENTAUREA BENEDICTA (UNII: 6L5ZL09795) (CENTAUREA BENEDICTA - UNII:6L5ZL09795) CENTAUREA BENEDICTA 0.0231 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Aloe Vera Leaf (UNII: ZY81Z83H0X) Propanediol (UNII: 5965N8W85T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72186-011-11 30 mL in 1 JAR; Type 0: Not a Combination Product 12/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 12/02/2019 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 liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72186-012 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 6 [hp_X] in 1 mL CALCIUM PHOSPHATE, UNSPECIFIED FORM (UNII: 97Z1WI3NDX) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM PHOSPHATE, UNSPECIFIED FORM 6 [hp_X] in 1 mL CALCIUM SULFATE, UNSPECIFIED FORM (UNII: WAT0DDB505) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE, UNSPECIFIED FORM 6 [hp_X] in 1 mL FERROUS PHOSPHATE (UNII: D07L04MRWI) (FERROUS CATION - UNII:GW89581OWR) FERROUS PHOSPHATE 6 [hp_X] in 1 mL MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE (UNII: 453COF7817) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE 6 [hp_X] in 1 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 6 [hp_X] in 1 mL DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR, POTASSIUM CATION - UNII:295O53K152) DIBASIC POTASSIUM PHOSPHATE 6 [hp_X] in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 6 [hp_X] in 1 mL SODIUM PHOSPHATE (UNII: SE337SVY37) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE 6 [hp_X] in 1 mL SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 6 [hp_X] in 1 mL HYDRATED SILICA (UNII: Y6O7T4G8P9) (HYDRATED SILICA - UNII:Y6O7T4G8P9) HYDRATED SILICA 6 [hp_X] in 1 mL CENTAUREA BENEDICTA (UNII: 6L5ZL09795) (CENTAUREA BENEDICTA - UNII:6L5ZL09795) CENTAUREA BENEDICTA 0.0231 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Alcohol (UNII: 3K9958V90M) Propanediol (UNII: 5965N8W85T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72186-012-12 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 12/02/2019 Labeler - Key Origins, Inc. (072533626) Establishment Name Address ID/FEI Business Operations Key Origins, Inc. 072533626 MANUFACTURE(72186-011, 72186-012) , PACK(72186-011, 72186-012)