FDA.reportPublic FDA data

Homeopathic Moon drops - Historical Remedies LLP

Manufacturer
Historical Remedies LLP
Effective date
2026-10-29
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-11-03 06:06:59

Label at a glance#

ProductHomeopathic Moon drops
Active ingredientARSENIC TRIOXIDE, MATRICARIA CHAMOMILLA WHOLE, ARABICA COFFEE BEAN, GELSEMIUM SEMPERVIRENS ROOT, STRYCHNOS IGNATII SEED, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, VALERIAN
Label structure6 sections

Dosage and administration

Adults and children over 8: Dissolve one Moon Drops lozenge in mouth. Repeat every half hour as needed.

Label contents#

Full prescribing information#

Indication

INDICATIONS & USAGE SECTION

Helps relieve occasional sleeplessness by soothing the mind, and easing you into a natural sleep. These uses are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 8: Dissolve one Moon Drops lozenge in mouth. Repeat every half hour as needed.

Warnings

WARNINGS SECTION

If symptoms persist more than 7 days or worsen, consult a physician. Keep out of children’s reach.In case of overdose, get medical help or contact a poison control center right away. I f pregnant or breast-feeding, ask a doctor before use.
Do not use if shrink wrap is broken or missing.

Active Ingredients (HPUS)

OTC - ACTIVE INGREDIENT SECTION

Arsenicum alb 30X, Chamomilla 6X, Coffea cruda 12X, Gelsemium 12C, Ignatia 30X, Lycopodium 30X, Nat mur 30X, Nux vom 30X, Valeriana 12C. 

Inctive Ingredients

INACTIVE INGREDIENT SECTION

Dextrose Monohydrate, Magnesium Stearate, Maltodextrin, Organic Vanilla Flavor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57556-00857556-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARSENIC TRIOXIDES7V92P67HOACTIB
MATRICARIA CHAMOMILLA WHOLEG0R4UBI2ZZACTIB
ARABICA COFFEE BEAN3SW678MX72ACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
VALERIANJWF5YAW3QWACTIB
DEXTROSE MONOHYDRATELX22YL083GIACT
MAGNESIUM STEARATE70097M6I30IACT
MALTODEXTRIN7CVR7L4A2DIACT
ACHLYS TRIPHYLLA WHOLE91THU5EJ2IIACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72025-10-07full-release2026-06-01 01:41:49
62024-10-31full-release2026-06-01 00:33:34

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
4093ed93-db56-dfa6-e063-6394a90ad1370e7972a5-a930-4a52-8896-02ce810fa90b2025-10-07WarningsExact identifier
spl set id: 0e7972a5-a930-4a52-8896-02ce810fa90b

Reported adverse events (FAERS/openFDA)#

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