FDA.reportPublic FDA data

Nosebleed Relief

Manufacturer
King Bio Inc.
Effective date
2016-03-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:07:32

Label at a glance#

ProductNosebleed Relief
Active ingredientAMBROSIA ARTEMISIIFOLIA, ARNICA MONTANA, LYCOPERDON UTRIFORME FRUITING BODY, BRYONIA ALBA ROOT, ACTIVATED CHARCOAL, FERROSOFERRIC PHOSPHATE, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, IPECAC, MERCURY, NITRIC ACID, PHOSPHORUS, TRILLIUM ERECTUM ROOT
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: ​Ambrosia artemisiaefolia, Arnica montana, Bovista, Bryonia, Carbo vegetabilis, Ferrum phosphoricum, Hamamelis virginiana, Ipecacuanha, Mercurius vivus, Nitricum acidum, Phosphorus, Trillium pendulum​. Equal volumes of each ingredient in 10X, 30X, LM1 potencies.

INDICATIONS & USAGE SECTION

Uses ​for temporary relief of nosebleeds commonly associated with irritations or strains, colds, coughing, sneezing or menses.

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 2-12: 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 nosebleeds commonly associated with:

  • irritations or strains
  • colds
  • coughing
  • sneezing or menses

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-5140-22020-01-31C16284748780-19d75b9d0-070c-f424-e053-dadaa90a57ceNosebleed Relief™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-5140-2Nosebleed Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-5140NOSEBLEED RELIEF (AMBROSIA ARTEMISIAEFOLIA, ARNICA MONTANA, BOVISTA, BRYONIA, CARBO VEGETABILIS, FERRUM PHOSPHORICUM, HAMAMELIS VIRGINIANA, IPECACUANHA, MERCURIUS VIVUS, NITRICUM ACIDUM, PHOSPHORUS, TRILLIUM PENDULUM) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20160308_94ef9773-445f-4d3b-a9cb-59966e085304.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-514057955-5140-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMBROSIA ARTEMISIIFOLIA9W34L2CQ9AACTIB
ARNICA MONTANAO80TY208ZWACTIB
LYCOPERDON UTRIFORME FRUITING BODYK2A74U428FACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
FERROSOFERRIC PHOSPHATE91GQH8I5F7ACTIB
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKT7S323PKJSACTIB
IPECAC62I3C8233LACTIB
MERCURYFXS1BY2PGLACTIB
NITRIC ACID411VRN1TV4ACTIB
PHOSPHORUS27YLU75U4WACTIB
TRILLIUM ERECTUM ROOTAHW6F0T2X0ACTIB
WATER059QF0KO0RIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POTASSIUM SORBATE1VPU26JZZ4IACT

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
b0a44b5a-69d4-488a-9ea1-35254baee94494ef9773-445f-4d3b-a9cb-59966e0853042016-03-08WarningsExact identifier
spl id: b0a44b5a-69d4-488a-9ea1-35254baee944
spl set id: 94ef9773-445f-4d3b-a9cb-59966e085304

Reported adverse events (FAERS/openFDA)#

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