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 ID63479-0405_b9d0ffcf-f638-5b1b-e053-2a95a90aa8f9
NDC63479-0405
Product TypeHuman Otc Drug
Proprietary NameD05 KDNY-DRN
Generic NameApis 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 FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1993-03-15
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameApex Energetics Inc.
Substance NameAPIS 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 Strength15 [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 FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63479-0405-1

30 mL in 1 BOTTLE, GLASS (63479-0405-1)
Marketing Start Date1993-03-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63479-0405-1 [63479040501]

D05 KDNY-DRN SOLUTION
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1993-03-15

Drug Details


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