Claustrophobia

Manufacturer
King Bio Inc.
Effective date
2016-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:23

Label at a glance#

ProductClaustrophobia
Active ingredientACONITUM NAPELLUS, ANGELICA ARCHANGELICA ROOT, SILVER NITRATE, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, BLACK COHOSH, HYPERICUM PERFORATUM, LOBELIA CARDINALIS, MALUS DOMESTICA FLOWER, ACHILLEA MILLEFOLIUM, NITRIC ACID, PULSATILLA VULGARIS, SAGE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: Aconitum napellus, Angelica archangelica, Argentum nitricum, Calendula officinalis, Chamomilla, Cimicifuga racemosa, Lobelia cardinalis, Malus pumila, flos, Millefolim, Nitricum acidum, Pulsatilla, Salvia officinalis​. Equal volumes of each ingredient in 10X, 30X, 100X, 1LM, 2LM, 3LM, 5LM potencies.

INDICATIONS & USAGE SECTION

Uses for symptomatic relief of: claustrophobia, panic, nervous tension.

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, take only on advice of a healthcare professional.

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.
  • Adults: 3 sprays 3 times per day.
  • Children (2-12 years): 2 sprays 3 times per day.
  • ​Use additionally as needed, up to 6 times per day.

OTHER SAFETY INFORMATION

Tamper resistant for your protection. Use only if safety seal is intact. This product has not been clinically tested.

OTC - PURPOSE SECTION

Uses ​for symptomatic relief of:

  • claustrophobia
  • panic
  • nervous tension

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-1822-22020-01-31C16284748780-19d75b9cf-ed17-f424-e053-dadaa90a57ceClaustrophobia™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-1822-2Claustrophobia59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-1822CLAUSTROPHOBIA (ACONITUM NAPELLUS, ANGELICA ARCHANGELICA, ARGENTUM NITRICUM, CALENDULA OFFICINALIS, CHAMOMILLA, CIMICIFUGA RACEMOSA, HYPERICUM PERFORATUM, LOBELIA CARDINALIS, MALUS PUMILA, FLOS, MILLEFOLIUM, NITRICUM ACIDUM, PULSATILLA, SALVIA OFFICINALIS) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20161202_1dcfcd7c-07fa-4e3d-a074-88a8e4075cdc.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
57955-182257955-1822-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
7209b2cd-bd6d-4415-bd2e-a5d3629816671dcfcd7c-07fa-4e3d-a074-88a8e4075cdc2016-12-02WarningsExact identifier
spl id: 7209b2cd-bd6d-4415-bd2e-a5d362981667
spl set id: 1dcfcd7c-07fa-4e3d-a074-88a8e4075cdc

Reported adverse events (FAERS/openFDA)#

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