FDA.reportPublic FDA data

beyond heartbreak

Manufacturer
JMSP USA LLC | W Last CC
Effective date
2017-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:50

Label at a glance#

Productbeyond heartbreak
Active ingredientSTRYCHNOS IGNATII SEED, SODIUM CHLORIDE, ANEMONE PULSATILLA, DELPHINIUM STAPHISAGRIA SEED
Label structure8 sections

Indications and uses

Comfort and Support Following LOSS- BREAK UP DIVORCE ANXIETY BEREAVEMENT

Dosage and administration

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

Label contents#

Full prescribing information#

Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Ignatia (STRYCHNOS IGNATII SEED) 30 cH

NatrumMuriaticum (SODIUM CHLORIDE) 30 cH

Pulsatilla (ANEMONE PULSATILLA) 30 cH

Staphysagria (DELPHINIUM STAPHISAGRIA SEED) 30 cH

Purpose of ingredients:

OTC - PURPOSE SECTION

Comfort and Support Following LOSS- BREAK UP  DIVORCE ANXIETY BEREAVEMENT

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 physician prior to use.

Indications and Usage:

INDICATIONS & USAGE SECTION

Comfort and Support Following LOSS- BREAK UP DIVORCE ANXIETY BEREAVEMENT

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified Water and Ethyl Alcohol

Directions 

DOSAGE & ADMINISTRATION SECTION

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

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

heart breakheart breakheart break backheart break back

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58214-123-012020-01-31C16284748780-19d75b9cf-dc7c-f424-e053-dadaa90a57ceBeyond heartbreak

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58214-123-01beyond heartbreak30 mL in 1 PACKAGESPRAY301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58214-123BEYOND HEARTBREAK (IGNATIA, NATRUM MURIATICUM , PULSATILLA,STAPHYSAGRIA) SPRAY [JMSP USA LLC]1Legacy NDC, 1 package rows20170613_1caf2352-3eb5-4b0f-ad6f-735ef18cda49.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58214-12358214-123-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
DELPHINIUM STAPHISAGRIA SEED00543AP1JVACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
6d3701dc-cffc-4cce-8e55-77ebce864dfb1caf2352-3eb5-4b0f-ad6f-735ef18cda492017-06-12WarningsExact identifier
spl id: 6d3701dc-cffc-4cce-8e55-77ebce864dfb
spl set id: 1caf2352-3eb5-4b0f-ad6f-735ef18cda49

Reported adverse events (FAERS/openFDA)#

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