Label: D-TOX REMEDY- antimonium tartaricum, bromium, bryonia, carbo vegetabilis, carduus marianus, echinacea purpurea, hepar sulphuris calcareum, kali bichromicum, lobelia inflata, phosphorus, phytolacca decandra, silicea, solidago virgaurea, spongia tosta, sulphur iodatum liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53852-0005-4 - Packager: Living Well Remedies, LLC
- 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 May 8, 2014
If you are a consumer or patient please visit this version.
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DOSAGE & ADMINISTRATION
Directions: Take one teaspoon daily every evening, 30 minutes away from food or drink. Use a clean plastic teaspoon. One bottle lasts approximately one month. For maximum benefits, take daily for several months based on number (#) of years smoking:
Years Smoking = # months/bottles
1-5 years = 3 months/bottles
6-15 years = 6 months/bottles
16-20 years = 9 months/bottles
over 20 years =12 months/bottles
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- OTHER SAFETY INFORMATION
- PURPOSE
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ACTIVE INGREDIENT
Ingredients: Official HPUS: Antimonium tartaricum, Bromium, Bryonia, Carbo vegetabilis, Carduus marianus, Echinacea purpurea, Hepar sulphuris calcareum, Kali bichromicum, Lobelia inflata, Phosphorus, Phytolacca decandra, Silicea, Solidago virgaurea, Spongia tosta, Sulphur iodatum. Equal volumes of each ingredient in 10C, 30C, LM1 potencies.
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
D-TOX REMEDY
antimonium tartaricum, bromium, bryonia, carbo vegetabilis, carduus marianus, echinacea purpurea, hepar sulphuris calcareum, kali bichromicum, lobelia inflata, phosphorus, phytolacca decandra, silicea, solidago virgaurea, spongia tosta, sulphur iodatum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53852-0005 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 10 [hp_C] in 118 mL BROMINE (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G) BROMINE 10 [hp_C] in 118 mL BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 10 [hp_C] in 118 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 10 [hp_C] in 118 mL MILK THISTLE (UNII: U946SH95EE) (MILK THISTLE - UNII:U946SH95EE) MILK THISTLE 10 [hp_C] in 118 mL ECHINACEA PURPUREA (UNII: QI7G114Y98) (ECHINACEA PURPUREA - UNII:QI7G114Y98) ECHINACEA PURPUREA 10 [hp_C] in 118 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 10 [hp_C] in 118 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 10 [hp_C] in 118 mL LOBELIA INFLATA (UNII: 9PP1T3TC5U) (LOBELIA INFLATA - UNII:9PP1T3TC5U) LOBELIA INFLATA 10 [hp_C] in 118 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 10 [hp_C] in 118 mL PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 10 [hp_C] in 118 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 10 [hp_C] in 118 mL SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50) SOLIDAGO VIRGAUREA FLOWERING TOP 10 [hp_C] in 118 mL SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 10 [hp_C] in 118 mL SULFUR IODIDE (UNII: L6L8KA2AA0) (SULFUR IODIDE - UNII:L6L8KA2AA0) SULFUR IODIDE 10 [hp_C] in 118 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53852-0005-4 59 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/08/2014 Labeler - Living Well Remedies, LLC (022609201) Registrant - Living Well Remedies, LLC (022609201)
