FDA.reportPublic FDA data

Water Retention

Manufacturer
King Bio Inc.
Effective date
2016-06-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:00

Label at a glance#

ProductWater Retention
Active ingredientACETIC ACID, APIS MELLIFERA, APOCYNUM CANNABINUM ROOT, BERBERIS VULGARIS ROOT BARK, CHIOCOCCA ALBA ROOT, DIGITALIS, HELLEBORUS NIGER ROOT, CENTELLA ASIATICA, SODIUM CHLORIDE, OXYDENDRUM ARBOREUM LEAF, LEAD, SAMBUCUS NIGRA FLOWERING TOP, SOLIDAGO VIRGAUREA FLOWERING TOP, STROPHANTHUS HISPIDUS SEED
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: ​Aceticum acidum, Apis mellifica, Apocynum cannabinum, Berberis vulgaris, Cahinca, Digitalis purpurea, Helleborus niger, Hydrocotyle asiatica, Natrum muriaticum, Oxydendrum arboreum, Plumbum metallicum, Sambucus nigra, Solidago virgaurea, Strophanthus hispidus.​ Equal volumes of each ingredient in 10X, 30X, LM1 potencies.

INDICATIONS & USAGE SECTION

Uses for temporary relief of symptoms related to common water retention and edema in the hands, feet, legs, ankles, such as: swelling and puffiness, heat intolerance, abdominal bloating, fatigue, unquenchable thrist, suppressed urination.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

WARNINGS SECTION

Warnings

  • Stop use and ask your doctor if symptoms persist or worsen.
  • If pregnant or breast-feeding, ​ask  ​a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Initially, depress pump until primed.
  • Spray one dose directly into mouth.
  • Ages 12 and up: 3 sprays 3 times per day.

OTHER SAFETY INFORMATION

Tamper resistant for your protection. Use only if safety seal is intact.

OTC - PURPOSE SECTION

Uses for temporary relief of symptoms related to common water retention and edema in the hands, feet, legs, ankles, such as:

  • swelling and puffiness
  • heat intolerance
  • abdominal bloating
  • fatigue
  • unquenchable thrist
  • suppressed urination

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
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362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
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e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-5078-22020-01-31C16284748780-19d75b9d0-c4cc-f424-e053-dadaa90a57ceWater Retention™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-5078-2Water Retention59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-5078WATER RETENTION (ACETICUM ACIDUM, APIS MELLIFICA, APOCYNUM CANNABINUM, BERBERIS VULGARIS, CAHINCA, DIGITALIS PURPUREA, HELLEBORUS NIGER, HYDROCOTYLE ASIATICA, NATRUM MURIATICUM, OXYDENDRUM ARBOREUM, PLUMBUM METALLICUM, SAMBUCUS NIGRA, SOLIDAGO VIRGAUREA, STROPHANTHUS HISPIDUS) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20160622_711e8fd4-cc15-4e18-9edb-b8612a21e7e6.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-507857955-5078-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACETIC ACIDQ40Q9N063PACTIB
APIS MELLIFERA7S82P3R43ZACTIB
APOCYNUM CANNABINUM ROOT2F92409L9ZACTIB
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
CHIOCOCCA ALBA ROOTYC9M5WOW5VACTIB
DIGITALISF1T8QT9U8BACTIB
HELLEBORUS NIGER ROOT608DGJ6815ACTIB
CENTELLA ASIATICA7M867G6T1UACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
OXYDENDRUM ARBOREUM LEAF3QO999NVF5ACTIB
LEAD2P299V784PACTIB
SAMBUCUS NIGRA FLOWERING TOPCT03BSA18UACTIB
SOLIDAGO VIRGAUREA FLOWERING TOP5405K23S50ACTIB
STROPHANTHUS HISPIDUS SEEDMO892VI77KACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT

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
d0ad3d17-e4f5-4c03-888d-4774d9a64e81711e8fd4-cc15-4e18-9edb-b8612a21e7e62016-06-22WarningsExact identifier
spl id: d0ad3d17-e4f5-4c03-888d-4774d9a64e81
spl set id: 711e8fd4-cc15-4e18-9edb-b8612a21e7e6

Reported adverse events (FAERS/openFDA)#

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