NDC 60986-2000

ECHINACEA

Echinacea Angustifolia, Hamammelis Virginiana, Calcarea Phosphorica, Hydrastis Canadanesis, Senega Officinalis, Silicea, Conium, Aurum Muriaticum Natronatum, Calcarea Carbonica, Fucus Vesiculosus, Lac

ECHINACEA is a Oral Tablet, Orally Disintegrating in the Human Otc Drug category. It is labeled and distributed by Marco Pharma International Llc.. The primary component is Echinacea Angustifolia; Hamamelis Virginiana Root Bark/stem Bark; Tribasic Calcium Phosphate; Goldenseal; Polygala Senega Root; Silicon Dioxide; Conium Maculatum Flowering Top; Sodium Tetrachloroaurate; Oyster Shell Calcium Carbonate, Crude; Fucus Vesiculosus; Lachesis Muta Venom.

• Product ID: 60986-2000_1084b58e-310d-46c1-8a6c-0680132ba6e4
• NDC: 60986-2000
• Product Type: Human Otc Drug
• Proprietary Name: ECHINACEA
• Generic Name: Echinacea Angustifolia, Hamammelis Virginiana, Calcarea Phosphorica, Hydrastis Canadanesis, Senega Officinalis, Silicea, Conium, Aurum Muriaticum Natronatum, Calcarea Carbonica, Fucus Vesiculosus, Lac
• Dosage Form: Tablet, Orally Disintegrating
• Route of Administration: ORAL
• Marketing Start Date: 1992-03-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Marco Pharma International LLC.
• Substance Name: ECHINACEA ANGUSTIFOLIA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; TRIBASIC CALCIUM PHOSPHATE; GOLDENSEAL; POLYGALA SENEGA ROOT; SILICON DIOXIDE; CONIUM MACULATUM FLOWERING TOP; SODIUM TETRACHLOROAURATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; FUCUS VESICULOSUS; LACHESIS MUTA VENOM
• Active Ingredient Strength: 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 60986-2000-2

100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (60986-2000-2)

• Marketing Start Date: 1992-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60986-2000-2 [60986200002]

ECHINACEA TABLET, ORALLY DISINTEGRATING

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1992-03-01
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
ECHINACEA ANGUSTIFOLIA	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: 54d73223-75f2-43d8-a930-d770da3f23b8
• Manufacturer:
  • Marco Pharma International LLC.
• UNII:
  • ETJ7Z6XBU4
  • ZW3Z11D0JV
  • Q28R5GF371
  • M7T6H7D4IF
  • 7FT6QUT299
  • VSW71SS07I
  • 91D9GV0Z28
  • 2E32821G6I
  • 535G2ABX9M
  • T7S323PKJS
  • VB06AV5US8

NDC Crossover Matching brand name "ECHINACEA" or generic name "Echinacea Angustifolia, Hamammelis Virginiana, Calcarea Phosphorica, Hydrastis Canadanesis, Senega Officinalis, Silicea, Conium, Aurum Muriaticum Natronatum, Calcarea Carbonica, Fucus Vesiculosus, Lac"

NDC	Brand Name	Generic Name
60295-0101	ECHINACEA	echinacea angustifolia, hamammelis virginiana, calcarea phosphorica, hydrastis canadanesis, senega officinalis, silicea, conium, aurum muriaticum natronatum, calcarea carbonica, fucus vesiculosus, lachesis mutus
60986-2000	ECHINACEA	ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LAC
60986-2020	ECHINACEA	ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS