NDC 48951-3101

Cinnabar Dandelion

Cinnabar Dandelion

Cinnabar Dandelion is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Elymus Repens Root; Taraxacum Palustre Root; Ferrous Disulfide; Carbonate Ion; Mercuric Cation.

• Product ID: 48951-3101_6c54d80c-209f-f21d-e053-2991aa0aa023
• NDC: 48951-3101
• Product Type: Human Otc Drug
• Proprietary Name: Cinnabar Dandelion
• Generic Name: Cinnabar Dandelion
• 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: ELYMUS REPENS ROOT; TARAXACUM PALUSTRE ROOT; FERROUS DISULFIDE; CARBONATE ION; MERCURIC CATION
• Active Ingredient Strength: 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-3101-1

10 AMPULE in 1 BOX (48951-3101-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-3101-1 [48951310101]

Cinnabar Dandelion LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
ELYMUS REPENS ROOT	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 8c98dc38-773c-424f-9a03-f14d8574ad7b
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 132N09W4PR
  • 3IXW0F6P8W
  • ED30FJ8Y42
  • GCZ4W7077C
  • 7UJQ5OPE7D

NDC Crossover Matching brand name "Cinnabar Dandelion" or generic name "Cinnabar Dandelion"

NDC	Brand Name	Generic Name
48951-3101	Cinnabar Dandelion	Cinnabar Dandelion
48951-3225	Cinnabar Dandelion	Cinnabar Dandelion