FDA.reportPublic FDA data

Melancholic

Manufacturer
King Bio, Inc.
Effective date
2017-03-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:37

Label at a glance#

ProductMelancholic
Active ingredientALFALFA, AMMONIUM CARBONATE, DILL, ANTIMONY TRISULFIDE, GOLD, BENZOIC ACID, MAHONIA AQUIFOLIUM ROOT BARK, FAGUS SYLVATICA FLOWERING TOP, ILEX AQUIFOLIUM FLOWERING TOP, LYCOPODIUM CLAVATUM SPORE, ACHILLEA MILLEFOLIUM, HYDROCHLORIC ACID, SCABIES LESION LYSATE (HUMAN), SALIX ALBA FLOWERING TOP
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

HPUS active ingredients: Alfalfa, Ammonium carbonicum, Anethum graveolens, Antimonium crudum, Aurum metallicum, Benzoicum acidum, Berberis aquifolium, Fagus sylvatica, flos, Ilex aquifolium, flos, Lycopodium clavatum, Millefolium, Muriaticum acidum, Psorinum, Salix vitellina, flos.  Equal volumes of each ingredient in 10X, 30X, 100X, 1LM, 2LM, 3LM, 5LM potencies.

INDICATIONS & USAGE SECTION

Uses a natural aid for: pessimism, depression, melancholy, discontent, ill humor, gloominess.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Bio-Energetically Enhanced™ pure water, citric acid, potassium sorbate.

WARNINGS SECTION

Warnings

  • Stop use and ask your doctor if symptoms persist or worsen.
  • If pregnant or breastfeeding, 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 seal is intact.  This product has not been clinically tested.

OTC - PURPOSE SECTION

Uses a natural aid for:

  • pessimism
  • depression
  • melancholy
  • discontent
  • ill humor
  • gloominess

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130357955201021GTIN-13: 0357955201021
EAN-13: 0357955201021
GTIN-12: 357955201021
UPC-A: 357955201021
GTIN storage (14 digits): 00357955201021		Melancholic SCRX.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-2011-22020-01-31C16284748780-19d75b9cf-d1cc-f424-e053-dadaa90a57ceMelancholic™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-2011-2Melancholic59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-2011MELANCHOLIC (ALFALFA, AMMONIUM CARBONICUM, ANETHUM GRAVEOLENS, ANTIMONIUM CRUDUM, AURUM METALLICUM, BENZOICUM ACIDUM, BERBERIS AQUIFOLIUM, FAGUS SYLVATICA, FLOS, ILEX AQUIFOLIUM, FLOS, LYCOPODIUM CLAVATUM, MILLEFOLIUM, MURIATICUM ACIDUM, PSORINUM, SALIX VITELLINA, FLOS.) LIQUID [KING BIO, INC.]1Legacy NDC, 1 package rows20170310_dcd8d7f6-9f63-4b68-ad58-fd2b03ded000.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-201157955-2011-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALFALFADJO934BRBDACTIB
AMMONIUM CARBONATENJ5VT0FKLJACTIB
DILLY05PC4JZRHACTIB
ANTIMONY TRISULFIDEF79059A38UACTIB
GOLD79Y1949PYOACTIB
BENZOIC ACID8SKN0B0MIMACTIB
MAHONIA AQUIFOLIUM ROOT BARKVZJ9F3C3SBACTIB
FAGUS SYLVATICA FLOWERING TOP21AF0IHY5UACTIB
ILEX AQUIFOLIUM FLOWERING TOP5ENR9SAN1WACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
ACHILLEA MILLEFOLIUM2FXJ6SW4PKACTIB
HYDROCHLORIC ACIDQTT17582CBACTIB
SCABIES LESION LYSATE (HUMAN)5UAU16Z1U4ACTIB
SALIX ALBA FLOWERING TOPXBP5X7E70RACTIB
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
8f55da39-011a-414d-9163-96ddc02539d9dcd8d7f6-9f63-4b68-ad58-fd2b03ded0002017-03-10WarningsExact identifier
spl id: 8f55da39-011a-414d-9163-96ddc02539d9
spl set id: dcd8d7f6-9f63-4b68-ad58-fd2b03ded000

Reported adverse events (FAERS/openFDA)#

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