NDC 55714-6107

Bryonia

Bryonia

Bryonia is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Newton Laboratories, Inc.. The primary component is Bryonia Alba Root.

• Product ID: 55714-6107_373240cd-cd31-6695-e4c5-07bb1a1e9ee7
• NDC: 55714-6107
• Product Type: Human Otc Drug
• Proprietary Name: Bryonia
• Generic Name: Bryonia
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2011-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Newton Laboratories, Inc.
• Substance Name: BRYONIA ALBA ROOT
• Active Ingredient Strength: 15 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 55714-6107-1

30 mL in 1 BOTTLE, GLASS (55714-6107-1)

• Marketing Start Date: 2011-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55714-6107-1 [55714610701]

Bryonia LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-09-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
BRYONIA ALBA ROOT	15 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 152970d3-af84-42fc-2088-e332341a6642
• Manufacturer:
  • Newton Laboratories, Inc.
• UNII:
  • T7J046YI2B

NDC Crossover Matching brand name "Bryonia" or generic name "Bryonia"

NDC	Brand Name	Generic Name
0220-0915	Bryonia	BRYONIA ALBA ROOT
0220-0939	Bryonia	BRYONIA ALBA ROOT
0220-0940	Bryonia	BRYONIA ALBA ROOT
0220-0941	Bryonia	BRYONIA ALBA ROOT
0220-0942	Bryonia	BRYONIA ALBA ROOT
0220-0943	Bryonia	BRYONIA ALBA ROOT
0220-0944	Bryonia	BRYONIA ALBA ROOT
0220-0945	Bryonia	BRYONIA ALBA ROOT
0220-0946	Bryonia	BRYONIA ALBA ROOT
0220-0947	Bryonia	BRYONIA ALBA ROOT
0220-0948	Bryonia	BRYONIA ALBA ROOT
0220-0949	Bryonia	BRYONIA ALBA ROOT
0360-0076	BRYONIA	BRYONIA ALB.
0360-0077	BRYONIA	BRYONIA ALB.
44911-0382	Bryonia	Bryonia (Alba)
55714-6107	Bryonia	Bryonia
55714-9019	Bryonia	Bryonia
63083-7108	Bryonia	Bryonia