NDC 43742-0513

EBOLA REMEDY

Crotalus Horridus

EBOLA REMEDY is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Crotalus Horridus Horridus Venom.

• Product ID: 43742-0513_910330a0-332f-471c-aebb-b04ee7acd0a4
• NDC: 43742-0513
• Product Type: Human Otc Drug
• Proprietary Name: EBOLA REMEDY
• Generic Name: Crotalus Horridus
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-09-26
• Marketing End Date: 2022-10-06
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: CROTALUS HORRIDUS HORRIDUS VENOM
• Active Ingredient Strength: 8 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0513-1

30 mL in 1 BOTTLE, DROPPER (43742-0513-1)

• Marketing Start Date: 2014-09-26
• Marketing End Date: 2022-10-06
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0513-1 [43742051301]

EBOLA REMEDY LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-09-26
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CROTALUS HORRIDUS HORRIDUS VENOM	8 [hp_X]/mL

OpenFDA Data

• SPL SET ID: ab0ee604-99c0-49e2-b1b3-5765136f82d1
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • YHA2XLJ956

NDC Crossover Matching brand name "EBOLA REMEDY" or generic name "Crotalus Horridus"

NDC	Brand Name	Generic Name
43742-0513	EBOLA REMEDY	Crotalus Horridus
15631-0159	CROTALUS HORRIDUS	CROTALUS HORRIDUS
66096-825	Crotalus Horridus	CROTALUS HORRIDUS
69152-1106	Crotalus horridus 200C	Crotalus horridus