NDC 63479-0405

D05 KDNY-DRN

Apis Mellifera, Asparagus, Berberis Vulgaris Root Bark, Lytta Vesicatoria, Chelidonium Majus, Juniper Berry, Magnesium Chloride, Sodium Chloride, Populus Tremuloides Bark, Rhus Aromatica Root Bark, Rubia Tinctorum Root, Saw Palmetto, Solidago Virgaurea Flowering Top, Taraxacum Officinale, And Arctostaphylos Uva-ursi Leaf

D05 KDNY-DRN is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Apex Energetics Inc.. The primary component is Apis Mellifera; Asparagus; Berberis Vulgaris Root Bark; Lytta Vesicatoria; Chelidonium Majus; Juniper Berry; Magnesium Chloride; Sodium Chloride; Populus Tremuloides Bark; Rhus Aromatica Root Bark; Rubia Tinctorum Root; Saw Palmetto; Solidago Virgaurea Flowering Top; Taraxacum Officinale; Arctostaphylos Uva-ursi Leaf.

• Product ID: 63479-0405_b9d0ffcf-f638-5b1b-e053-2a95a90aa8f9
• NDC: 63479-0405
• Product Type: Human Otc Drug
• Proprietary Name: D05 KDNY-DRN
• Generic Name: Apis Mellifera, Asparagus, Berberis Vulgaris Root Bark, Lytta Vesicatoria, Chelidonium Majus, Juniper Berry, Magnesium Chloride, Sodium Chloride, Populus Tremuloides Bark, Rhus Aromatica Root Bark, Rubia Tinctorum Root, Saw Palmetto, Solidago Virgaurea Flowering Top, Taraxacum Officinale, And Arctostaphylos Uva-ursi Leaf
• Dosage Form: Solution
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 1993-03-15
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Apex Energetics Inc.
• Substance Name: APIS MELLIFERA; ASPARAGUS; BERBERIS VULGARIS ROOT BARK; LYTTA VESICATORIA; CHELIDONIUM MAJUS; JUNIPER BERRY; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; POPULUS TREMULOIDES BARK; RHUS AROMATICA ROOT BARK; RUBIA TINCTORUM ROOT; SAW PALMETTO; SOLIDAGO VIRGAUREA FLOWERING TOP; TARAXACUM OFFICINALE; ARCTOSTAPHYLOS UVA-URSI LEAF
• Active Ingredient Strength: 15 [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: 2022-12-31

Packaging

NDC 63479-0405-1

30 mL in 1 BOTTLE, GLASS (63479-0405-1)

• Marketing Start Date: 1993-03-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63479-0405-1 [63479040501]

D05 KDNY-DRN SOLUTION

• Marketing Category: Unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1993-03-15

Drug Details

Active Ingredients

Ingredient	Strength
APIS MELLIFERA	15 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 146800dc-bb1a-4d4c-803a-156a9fba600d
• Manufacturer:
  • Apex Energetics Inc.
• UNII:
  • 39981FM375
  • 3M5V3D1X36
  • 1TH8Q20J0U
  • 5405K23S50
  • 02F3473H9O
  • Q3H36W0J42
  • 7E889U5RNN
  • 451W47IQ8X
  • 0SVP95L23G
  • 5543O0CEID
  • J7WWH9M8QS
  • O84B5194RL
  • 3Q034RO3BT
  • 7S82P3R43Z
  • Z1EJP3037Z