FDA.reportPublic FDA data

Leptandra Combination

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:49:46

Label at a glance#

ProductLeptandra Combination 9230
Active ingredientVERONICASTRUM VIRGINICUM WHOLE, QUASSIA AMARA WOOD, VERATRUM ALBUM ROOT, ARSENIC TRIOXIDE, CEANOTHUS AMERICANUS LEAF, LYCOPODIUM CLAVATUM SPORE, MOMORDICA BALSAMINA WHOLE, PHOSPHORUS, PODOPHYLLUM, IODINE, MANDRAGORA OFFICINARUM ROOT, ACTIVATED CHARCOAL, NICKEL, SILVER NITRATE, MERCURIUS SOLUBILIS
Label structure9 sections

Dosage and administration

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Leptandra virginica 2X
Quassia amara 3X
Veratrum album 4X
Arsenicum album 6X
Ceanothus americanus 6X
Lycopodium clavatum 6X
Momordica balsamina 6X
Phosphorus 6X
Podophyllum peltatum 6X
Iodium 8X
Mandragora officinarum 8X
Carbo vegetabilis 10X
Niccolum metallicum 10X
Argentum nitricum 12X
Mercurius solubilis 12X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of diarrhea, stomach or abdominal cramping, flatulence, nausea, or vomiting.*

OTC - PURPOSE SECTION

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS

WARNINGS SECTION

If symptoms do not improve or are accompanied by a fever, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

40% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Leptandra Combination

Homeopathic Remedy

1 FL. OZ. (29.5 mL)

Label imageLabel image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-9230-12026-01-09C16284748780-11030e365-2fb4-111a-e063-dadaa90a10e2R230
63083-9230-12026-01-09C16284748780-11030e365-2fb4-111a-e063-dadaa90a10e2R230
63083-9230-12024-01-30C16284748780-11030e365-2fb4-111a-e063-dadaa90a10e2R230
63083-9230-12024-01-30C16284748780-11030e365-2fb4-111a-e063-dadaa90a10e2R230

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9230-1Leptandra Combination923029.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-923063083-9230-1

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
VERONICASTRUM VIRGINICUM WHOLE1RA4P35F0IACTIB
QUASSIA AMARA WOODS5249Q85HWACTIB
VERATRUM ALBUM ROOTQNS6W5US1ZACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
CEANOTHUS AMERICANUS LEAF25B1Y14T8NACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
MOMORDICA BALSAMINA WHOLEP5JFB9U0GMACTIB
PHOSPHORUS27YLU75U4WACTIB
PODOPHYLLUM2S713A4VP3ACTIB
IODINE9679TC07X4ACTIB
MANDRAGORA OFFICINARUM ROOTI2XCB174VBACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
NICKEL7OV03QG267ACTIB
SILVER NITRATE95IT3W8JZEACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:15:48

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
Leptandra Combination 9230LEPTANDRA COMBINATIONProfessional Complementary Health Formulas2ce3a622-3d59-4a95-9dc2-22cd55b994a62026-01-08WarningsExact identifier
ndc (package): 63083-9230-1
ndc (product): 63083-9230
ndc11 (package): 63083923001
spl id: 8ea62461-f8e5-453e-80f1-ea9f472416e6
spl set id: 2ce3a622-3d59-4a95-9dc2-22cd55b994a6

Reported adverse events (FAERS/openFDA)#

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