Hedera helix

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 02:09:44

Label at a glance#

ProductHedera helix

Active ingredientHEDERA HELIX FLOWERING TWIG

Label structure8 sections

Indications and uses

To relieve the symptoms of hemorrhoids.

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

HEDERA

USES

OTC - PURPOSE SECTION

To relieve the symptoms of hemorrhoids.

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:

HEDERA Hemorrhoids

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 HEDERA is 3x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.
Availability is subject to change.

Hedera 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
NDC	Effective	Action	Document	Indexing SPL	Related label
71919-334-07	2020-01-31	C162847	48780-1	9d75b9d0-50e9-f424-e053-dadaa90a57ce	DRUG FACTS
71919-334-08	2020-01-31	C162847	48780-1	9d75b9d0-50e9-f424-e053-dadaa90a57ce	DRUG FACTS
71919-334-09	2020-01-31	C162847	48780-1	9d75b9d0-50e9-f424-e053-dadaa90a57ce	DRUG FACTS
71919-334-10	2020-01-31	C162847	48780-1	9d75b9d0-50e9-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71919-334-07	Hedera helix	15 mL in 1 VIAL, GLASS	LIQUID	15	1
71919-334-08	Hedera helix	30 mL in 1 VIAL, GLASS	LIQUID	30	1
71919-334-09	Hedera helix	50 mL in 1 BOTTLE, GLASS	LIQUID	50	1
71919-334-10	Hedera helix	100 mL in 1 BOTTLE, GLASS	LIQUID	100	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71919-334	HEDERA HELIX (HEDERA HELIX FLOWERING TWIG) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS]	1	Legacy NDC, 4 package rows	20180516_90f91e88-2973-4144-8a93-7c7abf161ffa.zip

Products#

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

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

Hedera helix
HEDERA HELIX FLOWERING TWIG
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71919-334	71919-334-07, 71919-334-08, 71919-334-09, 71919-334-10

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
Name	UNII	Kind
HEDERA HELIX FLOWERING TWIG	3D10KUA6BM	ACTIB
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
aa50e669-1339-436d-ba6c-486c8d6f22cc			90f91e88-2973-4144-8a93-7c7abf161ffa	2010-02-03	Warnings	Exact identifier spl id: aa50e669-1339-436d-ba6c-486c8d6f22cc spl set id: 90f91e88-2973-4144-8a93-7c7abf161ffa

Reported adverse events (FAERS/openFDA)#

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