NDC 48951-8306

Ignatia Bryophyllum

Ignatia Bryophyllum

Ignatia Bryophyllum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Strychnos Ignatii Seed; Lachesis Muta Venom; Silver; Kalanchoe Daigremontiana Leaf.

• Product ID: 48951-8306_6ac52a4d-c11a-560e-e053-2a91aa0a12b7
• NDC: 48951-8306
• Product Type: Human Otc Drug
• Proprietary Name: Ignatia Bryophyllum
• Generic Name: Ignatia Bryophyllum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc.
• Substance Name: STRYCHNOS IGNATII SEED; LACHESIS MUTA VENOM; SILVER; KALANCHOE DAIGREMONTIANA LEAF
• Active Ingredient Strength: 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-8306-3

60 mL in 1 BOTTLE, DROPPER (48951-8306-3)

• Marketing Start Date: 2009-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48951-8306-3 [48951830603]

Ignatia Bryophyllum LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-09-01

Drug Details

Active Ingredients

Ingredient	Strength
STRYCHNOS IGNATII SEED	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 39bd979f-919e-0554-e054-00144ff8d46c
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • VSW71SS07I
  • L6X13JKL8O
  • 1NM3M2487K
  • 3M4G523W1G

NDC Crossover Matching brand name "Ignatia Bryophyllum" or generic name "Ignatia Bryophyllum"

NDC	Brand Name	Generic Name
48951-5068	Ignatia Bryophyllum	Ignatia Bryophyllum
48951-5069	Ignatia Bryophyllum	Ignatia Bryophyllum
48951-8306	Ignatia Bryophyllum	Ignatia Bryophyllum