NDC 64578-0103

Renapath

Benzoicum Acidum, Berberis Vulgaris, Bryonia, Dna, Eupatorium Purpureum, Glandula Suprarenalis Suis, Hydrangea Arborescens, Hypothalamus, Mercurius Corrosivus, Pancreas Suis, Pareira Brava, Petroselinum Sativum, Pituitarum Posterium, Rubia Tinctorum, Sarsaparilla, Solidago Virgaurea, Thyroidinum (bovine), Uva-ursi

Renapath is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energetix Corp. The primary component is Benzoic Acid; Berberis Vulgaris Root Bark; Bryonia Alba Root; Herring Sperm Dna; Eutrochium Purpureum Root; Sus Scrofa Adrenal Gland; Hydrangea Arborescens Root; Bos Taurus Hypothalamus; Mercuric Chloride; Sus Scrofa Pancreas; Chondrodendron Tomentosum Root; Petroselinum Crispum; Sus Scrofa Pituitary Gland; Rubia Tinctorum Root; Sarsaparilla; Solidago Virgaurea Flowering Top; Thyroid, Bovine; Arctostaphylos Uva-ursi Leaf.

• Product ID: 64578-0103_3183420d-f221-4c9a-8bc6-7844370ba38a
• NDC: 64578-0103
• Product Type: Human Otc Drug
• Proprietary Name: Renapath
• Generic Name: Benzoicum Acidum, Berberis Vulgaris, Bryonia, Dna, Eupatorium Purpureum, Glandula Suprarenalis Suis, Hydrangea Arborescens, Hypothalamus, Mercurius Corrosivus, Pancreas Suis, Pareira Brava, Petroselinum Sativum, Pituitarum Posterium, Rubia Tinctorum, Sarsaparilla, Solidago Virgaurea, Thyroidinum (bovine), Uva-ursi
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-06-06
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Energetix Corp
• Substance Name: BENZOIC ACID; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; HERRING SPERM DNA; EUTROCHIUM PURPUREUM ROOT; SUS SCROFA ADRENAL GLAND; HYDRANGEA ARBORESCENS ROOT; BOS TAURUS HYPOTHALAMUS; MERCURIC CHLORIDE; SUS SCROFA PANCREAS; CHONDRODENDRON TOMENTOSUM ROOT; PETROSELINUM CRISPUM; SUS SCROFA PITUITARY GLAND; RUBIA TINCTORUM ROOT; SARSAPARILLA; SOLIDAGO VIRGAUREA FLOWERING TOP; THYROID, BOVINE; ARCTOSTAPHYLOS UVA-URSI LEAF
• Active Ingredient Strength: 10 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 64578-0103-1

59.1 mL in 1 BOTTLE, DROPPER (64578-0103-1)

• Marketing Start Date: 2017-07-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 64578-0103-1 [64578010301]

Renapath LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-07-13

Drug Details

Active Ingredients

Ingredient	Strength
BENZOIC ACID	10 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 1a37b994-9470-4266-a4e1-008538ea0edf
• Manufacturer:
  • Energetix Corp
• UNII:
  • 395A3P448Z
  • MN18OTN73W
  • 1TH8Q20J0U
  • S6G2NLH4Y7
  • SFK828Q2DE
  • 3M5V3D1X36
  • 53GH7MZT1R
  • 0SVP95L23G
  • 51FI676N6F
  • 398IYQ16YV
  • 2H1576D5WG
  • T7J046YI2B
  • 0VYG5PVN5Q
  • 5405K23S50
  • 9Y3J3362RY
  • 8SKN0B0MIM
  • L0PFEMQ1DT
  • 1WZA4Y92EX
• UPC Code:
  • 0364578040715