FDA.reportPublic FDA data

Ailanthus glandulosus

Manufacturer
Washington Homeopathic Products
Effective date
2018-12-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:34:45

Label at a glance#

ProductAilanthus glandulosus
Active ingredientAILANTHUS ALTISSIMA FLOWERING TWIG
Label structure8 sections

Indications and uses

To relieve the symptoms of red eruptions.

Dosage and administration

Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

AILANTHUS

USES

OTC - PURPOSE SECTION

To relieve the symptoms of red eruptions.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications: 

AILANTHUS   Red eruptions

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The OTC potency range of AILANTHUS is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

LabelLabel

All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.

‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.

Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71919-025-072022-03-25C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS
71919-025-082022-03-25C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS
71919-025-092022-03-25C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS
71919-025-102022-03-25C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS
71919-025-072020-01-31C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS
71919-025-082020-01-31C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS
71919-025-092020-01-31C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS
71919-025-102020-01-31C16284748780-19d75b9d0-cbe0-f424-e053-dadaa90a57ceDRUG FACTS

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71919-02571919-025-07, 71919-025-08, 71919-025-09, 71919-025-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
AILANTHUS ALTISSIMA FLOWERING TWIG8P29O5P7XUACTIB

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
db0d0e48-566b-ece0-e053-2a95a90ad597cff2f89e-cfda-41c6-80c0-316533c1fe032022-03-25WarningsExact identifier
spl set id: cff2f89e-cfda-41c6-80c0-316533c1fe03

Reported adverse events (FAERS/openFDA)#

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