NDC 60986-1004

Lymphonest

Echinacea Augustifolia, Scrophularia Nodosa, Abrotanum, Petroleum, Aloe Socotrina, Mercurius Solubilis, Crotalus Horiidus, Thuja Occidentalis, Lachesis Mutus, Aristolochia Clematitis

Lymphonest is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Marco Pharma International Llc.. The primary component is Echinacea Angustifolia; Scrophularia Nodosa; Artemisia Abrotanum Flowering Top; Kerosene; Aloe; Mercurius Solubilis; Crotalus Horridus Horridus Venom; Thuja Occidentalis Leafy Twig; Lachesis Muta Venom; Aristolochia Clematitis Root.

Product ID60986-1004_3309a9ca-7ff5-4b56-bf2d-7d0e26eaf143
NDC60986-1004
Product TypeHuman Otc Drug
Proprietary NameLymphonest
Generic NameEchinacea Augustifolia, Scrophularia Nodosa, Abrotanum, Petroleum, Aloe Socotrina, Mercurius Solubilis, Crotalus Horiidus, Thuja Occidentalis, Lachesis Mutus, Aristolochia Clematitis
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1992-03-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameMarco Pharma International LLC.
Substance NameECHINACEA ANGUSTIFOLIA; SCROPHULARIA NODOSA; ARTEMISIA ABROTANUM FLOWERING TOP; KEROSENE; ALOE; MERCURIUS SOLUBILIS; CROTALUS HORRIDUS HORRIDUS VENOM; THUJA OCCIDENTALIS LEAFY TWIG; LACHESIS MUTA VENOM; ARISTOLOCHIA CLEMATITIS ROOT
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 60986-1004-3

50 mL in 1 BOTTLE, GLASS (60986-1004-3)
Marketing Start Date2018-02-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60986-1004-3 [60986100403]

Lymphonest LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-02-28
Inactivation Date2020-01-31

NDC 60986-1004-4 [60986100404]

Lymphonest LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-02-28
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ECHINACEA ANGUSTIFOLIA1 [hp_X]/100mL

OpenFDA Data

SPL SET ID:84e18e97-4892-4699-b0c6-c194dc783b2d
Manufacturer
UNII

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