NDC 48951-3102

Cinnabar Dandelion Cold Relief

Taraxacum Officinale Elymus Repens Root Potash Mercuric Sulfide

Cinnabar Dandelion Cold Relief is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc. The primary component is Taraxacum Officinale; Elymus Repens Root; Potash; Mercuric Sulfide.

• Product ID: 48951-3102_a8f9adb0-f62d-11de-8a39-0800200c9a66
• NDC: 48951-3102
• Product Type: Human Otc Drug
• Proprietary Name: Cinnabar Dandelion Cold Relief
• Generic Name: Taraxacum Officinale Elymus Repens Root Potash Mercuric Sulfide
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc
• Substance Name: TARAXACUM OFFICINALE; ELYMUS REPENS ROOT; POTASH; MERCURIC SULFIDE
• Active Ingredient Strength: 2 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 48951-3102-2

1350 PELLET in 1 BOTTLE, GLASS (48951-3102-2)

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

NDC SPL Data Element Entries

NDC 48951-3102-2 [48951310202]

Cinnabar Dandelion Cold Relief PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-09-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
TARAXACUM OFFICINALE	2 [hp_X]/1

OpenFDA Data

• SPL SET ID: 483bf242-df66-11de-8a39-0800200c9a66
• Manufacturer:
  • Uriel Pharmacy Inc
• UNII:
  • 39981FM375
  • ZI0T668SF1
  • 3IXW0F6P8W