NDC 48951-3108

Cocculus Conium Special Order

Cocculus Conium Special Order

Cocculus Conium Special Order is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Anamirta Cocculus Whole; Conium Maculatum Root; Ambergris; Liquid Petroleum.

• Product ID: 48951-3108_6cd08de1-4686-4776-e053-2a91aa0ab611
• NDC: 48951-3108
• Product Type: Human Otc Drug
• Proprietary Name: Cocculus Conium Special Order
• Generic Name: Cocculus Conium Special Order
• 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: ANAMIRTA COCCULUS WHOLE; CONIUM MACULATUM ROOT; AMBERGRIS; LIQUID PETROLEUM
• 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 48951-3108-1

10 AMPULE in 1 BOX (48951-3108-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-3108-1 [48951310801]

Cocculus Conium Special Order LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
ANAMIRTA COCCULUS WHOLE	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 86212fdd-6bb7-4c5d-ba59-2c4823d1de8d
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 8O4P2U3QO2
  • 6ZAE7X688J
  • XTC0D02P6C
  • TTE3RU7P5P