Bladder Urinary

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2024-11-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:28:44

Label at a glance#

ProductBladder Urinary
Active ingredientAPIS MELLIFERA, BERBERIS VULGARIS ROOT BARK, LYTTA VESICATORIA, PROTORTONIA CACTI, ECHINACEA ANGUSTIFOLIA WHOLE, EQUISETUM HYEMALE WHOLE, STRYCHNOS NUX-VOMICA SEED, RUBIA TINCTORUM ROOT, SMILAX ORNATA ROOT, DELPHINIUM STAPHISAGRIA SEED, THUJA OCCIDENTALIS LEAF, GINGER
Label structure9 sections

Indications and uses

May temporarily relieve these urinary symptoms: burning sensation frequent need to urinate painful urination** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

Adults and children over 12: Spray twice under the tongue three times per day. For severe symptoms, dosage may be taken up to six times the first day. Continue dosage for fourteen days after symptoms have subsided.  Children 12 and under: Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 8.33% of Apis Mellifica 200C, Berberis Vulgaris 6X, Cantharis 200C, Coccus Cacti 3X, Echinacea (Angustifolia) 1X, Equisetum Hyemale 6X, Nux Vomica 30C, Rubia Tinctorum 1X, Sarsaparilla (Smilax Regelii) 6X, Staphysagria 12C, Thuja Occidentalis 200C, Zingiber Officinale 6X.

USES:

OTC - PURPOSE SECTION

May temporarily relieve these urinary symptoms:

  • burning sensation
  • frequent need to urinate
  • painful urination**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

Do not use if you have ever has an allergic reaction to this product or any of its ingredients.

Stop use and ask a doctor if symptoms persist for more than 3 days, are severe, or you experience fever, chills, back pain or bloody urine.

You may have a serious condition that requires professional treatment.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

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

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Spray twice under the tongue three times per day.

For severe symptoms, dosage may be taken up to six times the first day. Continue dosage for fourteen days after symptoms have subsided. 

Children 12 and under: Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve these urinary symptoms:

• burning sensation
• frequent need to urinate
• painful urination**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified Water.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY

LIDDELL LABORATORIES INC.

201 APPLE BLVD.

WOODBINE, IA 51579

WWW.LIDDELL.NET

1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL

LABORATORIES

EST 1994

04 BI+

Bladder +

Urinary

May relieve urinary symptoms:

burning, frequent  + painful

urination.

HOMEOPATHIC

DOCTOR FORMULATED

Readily absorbed. Safe.

No known side effects. Easy to use.

1.0 FL OZ. (30ml)

Bladder + Urinary lblBladder + Urinary lbl

Bladder + Urinary ctnBladder + Urinary ctn

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0244-12024-11-04C16284748780-1ba0f9c33-2e65-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0244-12024-01-30C16284748780-1ba0f9c33-2e65-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0244-12022-04-19C16284748780-1ba0f9c33-2e65-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0244-12021-01-29C16284748780-1ba0f9c33-2e65-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50845-0244-1Bladder Urinary30 mL in 1 BOTTLE, SPRAYLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50845-0244BLADDER URINARY (APIS MELLIFICA, BERBERIS VULGARIS, CANTHARIS, COCCUS CACTI, ECHINACEA (ANGUSTIFOLIA), EQUISETUM HYEMALE, NUX VOMICA, RUBIA TINCTORUM, SARSAPARILLA, STAPHYSAGRIA, THUJA OCCIDENTALIS, ZINGIBER OFFICINALE) LIQUID [LIDDELL LABORATORIES, INC.]4Current NDC, Legacy NDC, 1 package rows20241105_3678b431-789e-453e-b5f4-5cf5b17ac0cc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-024450845-0244-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Bladder UrinaryAPIS MELLIFICA, BERBERIS VULGARIS, CANTHARIS, COCCUS CACTI, ECHINACEA (ANGUSTIFOLIA), EQUISETUM HYEMALE, NUX VOMICA, RUBIA TINCTORUM, SARSAPARILLA, STAPHYSAGRIA, THUJA OCCIDENTALIS, ZINGIBER OFFICINALELiddell Laboratories, Inc.3678b431-789e-453e-b5f4-5cf5b17ac0cc2024-11-04WarningsExact identifier
ndc (package): 50845-0244-1
ndc (product): 50845-0244
ndc11 (package): 50845024401
spl id: 82e09f62-3610-4b7c-aba4-b69b6e25b4eb
spl set id: 3678b431-789e-453e-b5f4-5cf5b17ac0cc

Reported adverse events (FAERS/openFDA)#

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