Snore Control

Manufacturer
King Bio Inc.
Effective date
2026-03-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:37:59

Label at a glance#

ProductSnore Control
Active ingredientBROMINE, MATRICARIA CHAMOMILLA WHOLE, CINCHONA OFFICINALIS BARK, COPPER, HELLEBORUS NIGER ROOT, HISTAMINE DIHYDROCHLORIDE, GOLDENSEAL, POTASSIUM DICHROMATE, PRUNUS LAUROCERASUS LEAF, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, DATURA STRAMONIUM, SULFUR, ZINC
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM potencies.

Bromium, Chamomilla, Cinchona, Cuprum metallicum, Helleborus niger, Histaminum hydrochloricum, Hydrastis canadensis, Kali bichromicum, Laurocerasus, Nux vomica, Phosphoricum acidum, Rhus tox, Silicea, Stramonium, Sulphur and Zincum metallicum.

** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″

INDICATIONS & USAGE SECTION

Uses † For temporary relief of symptoms related to snoring:

  • slow, labored breathing
  • stuffy nose, especially at night
  • heaviness of chest
  • dry cough

† Claims based on traditional Homeopathic practice, not accepted medical evidence, not
FDA evaluated.

Questions

OTC - QUESTIONS SECTION

Snore Control

Dr. King's Natural Medicine

Taste free, Pure Water Base

Oral Spray Tamper evident for your protection.

HOMEOPATHIC 2 fl oz (59 mL)

*Less than 1% Alcohol, Gluten Free

King Bio • 3 Westside Drive, Asheville, NC 28806 USA

www.DrKings.com
for additional information.

Scan and discover

Dr. King's FREE Videos and Home
Healing Techniques to integrate with
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healing experience.

Warnings

WARNINGS SECTION

  • Stop use and consult a doctor if symptoms worsen or persist for more than 7 days.
  • 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. In case of overdose, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions Oral Dose
 Adults and Children over 12
  •  2 sprays into mouth 3 to 6 times per day
 Children 6-12
  •  1 spray into mouth 3 to 6 times per day
 Children under 6
  • Do not use in children under 6, unless directed to by a doctor

OTHER SAFETY INFORMATION

Other information

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citric acid, Potassium sorbate, and USP purified water.

OTC - PURPOSE SECTION

Equal volumes of each HPUS ingredient in 10X, 30X, and 1LM
potencies.

Active ingredients                              Purpose †

Bromium ........................................jerking during sleep
Chamomilla........................................tightness of chest
Cinchona ........................snoring, slow labored breathing
Cuprum metallicum.................................tension in chest
Helleborus niger................................irregular respiration

Histaminum hydrochloricum .............inflammation, allergy
Hydrastis canadensis................................swollen tongue
Kali bichromicum ................swollen parotic glands, mucus
Laurocerasus ..........................snoring, dry, tickling cough
Nux vomica............................snoring with overindulgence
Phosphoricum acidum............................difficult breathing
Rhus tox ............................................heaviness of chest
Silicea ....................................coughing when lying down
Stramonium ...............................................deep snoring
Sulphur............snoring due to congestion, dryness or aging
Zincum metallicum.........................................hoarseness

** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″

† Claims based on traditional Homeopathic practice, not accepted medical evidence, not
FDA evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Snore Control.jpgSnore Control.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codedrkings.com/Snore Control.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-9983-2Snore Control59 mL in 1 BOTTLE, SPRAYLIQUID591

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-998357955-9983-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
Snore ControlBROMIUM, CHAMOMILLA, CINCHONA, CUPRUM METALLICUM, HELLEBORUS NIGER, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, LAUROCERASUS, NUX VOMICA, PHOSPHORICUM ACIDUM, RHUS TOX, SILICEA, STRAMONIUM, SULPHUR AND ZINCUM METALLICUM.King Bio Inc.704bb574-6c54-49d1-bdae-81ffe0e79d102026-03-04WarningsExact identifier
ndc (package): 57955-9983-2
ndc (product): 57955-9983
ndc11 (package): 57955998302
spl id: 6f361b61-60c1-4c90-8121-59b1a47c2197
spl set id: 704bb574-6c54-49d1-bdae-81ffe0e79d10

Reported adverse events (FAERS/openFDA)#

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