FDA.reportPublic FDA data

Dust Mite and Roach Allergy Relief

Manufacturer
King Bio Inc.
Effective date
2016-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:05

Label at a glance#

ProductDust Mite and Roach Allergy Relief
Active ingredientARALIA RACEMOSA ROOT, PERIPLANETA AMERICANA, BLATTA ORIENTALIS, CHELIDONIUM MAJUS, GOLDENSEAL, FLAX SEED, PHOSPHORUS, SULFUR, TRIFOLIUM PRATENSE FLOWER
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: ​Aralia racemosa, Blatta americana, Blatta orientalis, Chelidonium majus, Hydrastis canadensis, Linum usitatissimum, Phosphorus, Sulphur, Trifolium pratense. Equal volumes of each ingredient in 12X, 24X, LM1 potencies.

INDICATIONS & USAGE SECTION

Uses ​for temporary relief of symptoms related to dust mites and roaches: skin irritations, congestion, sneezing, minor respiratory difficulties, itchy, watery eyes, muscle and joint pain, coughing.

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.
  • Ages 3-12: 2 sprays 3 times per day.

OTHER SAFETY INFORMATION

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

OTC - PURPOSE SECTION

Uses for temporary relief of symptoms related to dust mites and roaches:

  • skin irritations
  • congestion
  • sneezing
  • minor respiratory difficulties
  • itchy, watery eyes
  • muscle and joint pain
  • coughing

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-6497-22020-01-31C16284748780-19d75b9d0-157f-f424-e053-dadaa90a57ceDust Mite and Roach Allergy Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-6497-2Dust Mite and Roach Allergy Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-6497DUST MITE AND ROACH ALLERGY RELIEF (ARALIA RACEMOSA, BLATTA AMERICANA, BLATTA ORIENTALIS, CHELIDONIUM MAJUS, HYDRASTIS CANADENSIS, LINUM USITATISSIMUM, PHOSPHORUS, SULPHUR, TRIFOLIUM PRATENSE) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20160713_677fb96a-eb18-435f-ade7-341ed64903a1.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-649757955-6497-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARALIA RACEMOSA ROOTT90W4582DUACTIB
PERIPLANETA AMERICANA2RQ1L9N089ACTIB
BLATTA ORIENTALIS535787266DACTIB
CHELIDONIUM MAJUS7E889U5RNNACTIB
GOLDENSEALZW3Z11D0JVACTIB
FLAX SEED4110YT348CACTIB
PHOSPHORUS27YLU75U4WACTIB
SULFUR70FD1KFU70ACTIB
TRIFOLIUM PRATENSE FLOWER4JS0838828ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
6d3c98c6-5c39-41be-83b4-5610e25514f5677fb96a-eb18-435f-ade7-341ed64903a12016-07-13WarningsExact identifier
spl id: 6d3c98c6-5c39-41be-83b4-5610e25514f5
spl set id: 677fb96a-eb18-435f-ade7-341ed64903a1

Reported adverse events (FAERS/openFDA)#

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