beyond insomnia

Manufacturer
JMSP USA LLC | W Last CC
Effective date
2013-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:50

Label at a glance#

Productbeyond insomnia
Active ingredientANAMIRTA COCCULUS SEED, COFFEA ARABICA SEED, ROASTED, STRYCHNOS NUX-VOMICA SEED
Label structure8 sections

Dosage and administration

One pump spray under the tongue up to 6 times a day, or as needed

Label contents#

Full prescribing information#

Active Ingrdietns 

OTC - ACTIVE INGREDIENT SECTION

Cocculus 30cH

Coffee tosta 30cH

nux vomica 30cH

Purpose 

OTC - PURPOSE SECTION

Promote sleep by calming the mind and body

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children

Warnings

WARNINGS SECTION

Not intended for pregnant or lactating women
Not to be taken by those with existing medical conditions, please consult your prior to use.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified Water, Ethyl Alcohol 15%

Directions 

DOSAGE & ADMINISTRATION SECTION

One pump spray under the tongue up to 6 times a day, or as needed

Usage

INDICATIONS & USAGE SECTION

Traditionally used to promote sleep by calming the mind and body

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

insomnia frontinsomnia frontinsomnia backinsomnia back

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58214-456-012020-01-31C16284748780-19d75b9cf-dc7f-f424-e053-dadaa90a57ceBeyond Insomnia

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58214-456-01beyond insomnia30 mL in 1 PACKAGESPRAY301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58214-456BEYOND INSOMNIA (COCCULUS, COFFEE TOSTA AND NUX VOMICA) SPRAY [JMSP USA LLC]1Legacy NDC, 1 package rows20170613_ddc74d7d-4a53-4050-a591-16366d1d1c8c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58214-45658214-456-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
d3e0fe2f-27e5-469d-b857-6d3b3ae227b5ddc74d7d-4a53-4050-a591-16366d1d1c8c2013-04-17WarningsExact identifier
spl id: d3e0fe2f-27e5-469d-b857-6d3b3ae227b5
spl set id: ddc74d7d-4a53-4050-a591-16366d1d1c8c

Reported adverse events (FAERS/openFDA)#

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