Passiflora incarnata

Manufacturer
Washington Homeopathic Products
Effective date
2010-02-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:43

Label at a glance#

ProductPassiflora incarnata
Active ingredientPASSIFLORA INCARNATA FLOWERING TOP
Label structure8 sections

Indications and uses

To relieve the symptoms of insomnia.

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

PASSIFLORA

USES

OTC - PURPOSE SECTION

To relieve the symptoms of insomnia.

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: 

PASSIFLORA   Insomnia

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 PASSIFLORA is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.
Availability is subject to change.

Passiflora label examplePassiflora label example

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
71919-521-072020-01-31C16284748780-19d75b9d0-2479-f424-e053-dadaa90a57ceDRUG FACTS
71919-521-082020-01-31C16284748780-19d75b9d0-2479-f424-e053-dadaa90a57ceDRUG FACTS
71919-521-092020-01-31C16284748780-19d75b9d0-2479-f424-e053-dadaa90a57ceDRUG FACTS
71919-521-102020-01-31C16284748780-19d75b9d0-2479-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71919-521-07Passiflora incarnata15 mL in 1 VIAL, GLASSLIQUID151
71919-521-08Passiflora incarnata30 mL in 1 VIAL, GLASSLIQUID301
71919-521-09Passiflora incarnata50 mL in 1 BOTTLE, GLASSLIQUID501
71919-521-10Passiflora incarnata100 mL in 1 BOTTLE, GLASSLIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71919-521PASSIFLORA INCARNATA (PASSIFLORA INCARNATA FLOWERING TOP) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS]1Legacy NDC, 4 package rows20180516_36aa97ae-25d9-4a67-94cf-5e888d0651d4.zip

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
71919-52171919-521-07, 71919-521-08, 71919-521-09, 71919-521-10

Ingredients#

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

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

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
9f7c6143-51a4-4122-89ba-59ccb1f7244836aa97ae-25d9-4a67-94cf-5e888d0651d42010-02-03WarningsExact identifier
spl id: 9f7c6143-51a4-4122-89ba-59ccb1f72448
spl set id: 36aa97ae-25d9-4a67-94cf-5e888d0651d4

Reported adverse events (FAERS/openFDA)#

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