NDC 48951-4090

Formica Oxalis

Formica Oxalis

Formica Oxalis is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Oxalis Acetosella Leaf; Formica Rufa.

• Product ID: 48951-4090_6dd4dbe0-aedd-5d6a-e053-2a91aa0aa106
• NDC: 48951-4090
• Product Type: Human Otc Drug
• Proprietary Name: Formica Oxalis
• Generic Name: Formica Oxalis
• 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: OXALIS ACETOSELLA LEAF; FORMICA RUFA
• Active Ingredient Strength: 3 [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-4090-2

1350 PELLET in 1 BOTTLE, GLASS (48951-4090-2)

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

NDC SPL Data Element Entries

NDC 48951-4090-2 [48951409002]

Formica Oxalis PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
OXALIS ACETOSELLA LEAF	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: 46f65e5b-6dc9-4582-a45f-8d3350de351f
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • U1W3U02EW0
  • 55H0W83JO5

NDC Crossover Matching brand name "Formica Oxalis" or generic name "Formica Oxalis"

NDC	Brand Name	Generic Name
48951-4089	Formica Oxalis	Formica Oxalis
48951-4090	Formica Oxalis	Formica Oxalis