NDC 66343-004

Paravita

Formica Rufa, Sus Scrofa Cerebellum, Acetylcholine, And Scabies Lesion Lysate (human)

Paravita is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Rubimed Ag. The primary component is Formica Rufa; Sus Scrofa Cerebellum; Acetylcholine; Scabies Lesion Lysate (human).

• Product ID: 66343-004_fbd55255-19c8-4811-a7c3-3ecdf217e948
• NDC: 66343-004
• Product Type: Human Otc Drug
• Proprietary Name: Paravita
• Generic Name: Formica Rufa, Sus Scrofa Cerebellum, Acetylcholine, And Scabies Lesion Lysate (human)
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-05-07
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: RUBIMED AG
• Substance Name: FORMICA RUFA; SUS SCROFA CEREBELLUM; ACETYLCHOLINE; SCABIES LESION LYSATE (HUMAN)
• Active Ingredient Strength: 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 66343-004-50

50 mL in 1 BOTTLE, DROPPER (66343-004-50)

• Marketing Start Date: 2015-05-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 66343-004-50 [66343000450]

Paravita LIQUID

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-05-07
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
FORMICA RUFA	12 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 30bf403b-5408-4089-af74-f06a78ce6214
• Manufacturer:
  • RUBIMED AG
• UNII:
  • N9YNS0M02X
  • 5UAU16Z1U4
  • 49NGK53TPQ
  • 55H0W83JO5

NDC Crossover Matching brand name "Paravita" or generic name "Formica Rufa, Sus Scrofa Cerebellum, Acetylcholine, And Scabies Lesion Lysate (human)"

NDC	Brand Name	Generic Name
66343-004	Paravita	Formica rufa, Sus Scrofa Cerebellum, Acetylcholine, and Scabies Lesion Lysate (Human)
66343-080	Paravita	Cerebrum, Formica rufa, Sulphur, Vespa crabro
66343-118	Paravita	Cerebrum, Formica rufa, Sulphur, Vespa crabro