NDC 48951-3046

Celandine Honey

Celandine Honey

Celandine Honey is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Chelidonium Majus; Honey.

• Product ID: 48951-3046_6a9cd70a-11ce-ae23-e053-2a91aa0a0c0f
• NDC: 48951-3046
• Product Type: Human Otc Drug
• Proprietary Name: Celandine Honey
• Generic Name: Celandine Honey
• 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: CHELIDONIUM MAJUS; HONEY
• Active Ingredient Strength: 4 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-3046-1

1 BOTTLE, DROPPER in 1 BAG (48951-3046-1) > 7 mL in 1 BOTTLE, DROPPER

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

NDC SPL Data Element Entries

NDC 48951-3046-1 [48951304601]

Celandine Honey LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
CHELIDONIUM MAJUS	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 503f666d-d51e-49fd-9312-3d54045d300e
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 7E889U5RNN
  • Y9H1V576FH

NDC Crossover Matching brand name "Celandine Honey" or generic name "Celandine Honey"

NDC	Brand Name	Generic Name
48951-3046	Celandine Honey	Celandine Honey
48951-3248	Celandine Honey	Celandine Honey