NDC 60986-1008

Cholenest

Rhamnus Purshiana, Carduus Marianus, Taraxacum Officinale, Chelidonium Majus, Leptandra Virginica, Myrica Cerifera, Berberis Vulgaris, Natrum Sulphuricum, Magnesia Phosphorica, Cuprum Metallicum

Cholenest is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Marco Pharma International Llc.. The primary component is Frangula Purshiana Bark; Silybum Marianum Seed; Taraxacum Officinale; Chelidonium Majus; Veronicastrum Virginicum Root; Morella Cerifera Root Bark; Berberis Vulgaris Root Bark; Sodium Sulfate; Magnesium Phosphate, Dibasic Trihydrate; Copper.

Product ID60986-1008_445b22ca-c426-4ab5-aaec-620e9dea3093
NDC60986-1008
Product TypeHuman Otc Drug
Proprietary NameCholenest
Generic NameRhamnus Purshiana, Carduus Marianus, Taraxacum Officinale, Chelidonium Majus, Leptandra Virginica, Myrica Cerifera, Berberis Vulgaris, Natrum Sulphuricum, Magnesia Phosphorica, Cuprum Metallicum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1992-03-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameMarco Pharma International LLC.
Substance NameFRANGULA PURSHIANA BARK; SILYBUM MARIANUM SEED; TARAXACUM OFFICINALE; CHELIDONIUM MAJUS; VERONICASTRUM VIRGINICUM ROOT; MORELLA CERIFERA ROOT BARK; BERBERIS VULGARIS ROOT BARK; SODIUM SULFATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; COPPER
Active Ingredient Strength1 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60986-1008-3

50 mL in 1 BOTTLE, GLASS (60986-1008-3)
Marketing Start Date2018-02-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60986-1008-4 [60986100804]

Cholenest LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-02-27
Inactivation Date2020-01-31

NDC 60986-1008-3 [60986100803]

Cholenest LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-02-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FRANGULA PURSHIANA BARK1 [hp_X]/100mL

OpenFDA Data

SPL SET ID:4b89ffcb-318b-416d-b13c-19fb94c2af70
Manufacturer
UNII

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