Kidney Drainage

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2018-10-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:49:17

Label at a glance#

ProductKidney Drainage
Active ingredientSOLIDAGO VIRGAUREA FLOWERING TOP, ASPARAGUS, JUNIPERUS COMMUNIS WHOLE, SAW PALMETTO, ARCTOSTAPHYLOS UVA-URSI LEAF, BERBERIS VULGARIS ROOT BARK, EQUISETUM ARVENSE TOP, RHUS AROMATICA ROOT BARK, URTICA DIOICA, LYTTA VESICATORIA, RUBIA TINCTORUM ROOT, DELPHINIUM STAPHISAGRIA SEED, COBALT, FAGUS SYLVATICA FLOWERING TOP, SUS SCROFA ADRENAL GLAND, CALCIUM SULFIDE, PORK KIDNEY, LARIX DECIDUA FLOWERING TOP, MANGANESE, MIMULUS GUTTATUS FLOWERING TOP, NITRIC ACID, SILICON DIOXIDE, ULEX EUROPAEUS FLOWER, BENZOIC ACID
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Solidago Virgaurea 1X, Asparagus Officinalis 2X, Juniperus Communis 2X, Sabal Serrulata 2X, Uva Ursi 2X, Berberis Vulgaris 3X, Equisetum Arvense 3X, Rhus Aromatica 3X, Urtica Dioica 3X, Cantharis 6X, Rubia Tinctorum 6X, Staphysagria 6X, Cobaltum Metallicum 6X, Fagus Sylvatica Flos 8X, Glandula Suprarenalis Suis 8X, Hepar Sulphuris Calcareum 8X, Kidney (Suis) 8X, Larix Decidua Flos 8X, Manganum Metallicum 8X, Mimulus Guttatus Flos 8X, Nitricum Acidum 8X, Silicea 8X, Ulex Europaeus Flos 8X, Benzoicum Acidum 12X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms related to kidney drainage, such as swelling and fatigue.**


**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms related to kidney drainage, such as swelling and fatigue.**


**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE DISPLAY LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0243-1

HOMEOPATHIC

KIDNEY

DRAINAGE

2 FL OZ (60 ml)

Kidney DrainageKidney Drainage

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-085843742-0858-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c6d48e78-b296-4d44-bbcc-8e289e1f5d30c666c68f-ad45-483a-96f8-c8255ab3688f2018-10-10WarningsExact identifier
spl id: c6d48e78-b296-4d44-bbcc-8e289e1f5d30
spl set id: c666c68f-ad45-483a-96f8-c8255ab3688f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.