NDC 48951-4089

Formica Oxalis

Formica Oxalis

Formica Oxalis is a Oral Liquid 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: 48951-4089_55b2af63-81b1-5c82-e054-00144ff88e88
• NDC: 48951-4089
• Product Type: Human Otc Drug
• Proprietary Name: Formica Oxalis
• Generic Name: Formica Oxalis
• 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: OXALIS ACETOSELLA LEAF; FORMICA RUFA
• Active Ingredient Strength: 3 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-4089-1

10 AMPULE in 1 BOX (48951-4089-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-4089-1 [48951408901]

Formica Oxalis LIQUID

• 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]/mL

OpenFDA Data

• SPL SET ID: 0c6612b0-773b-4943-b34b-156704a8714b
• 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