Abelmoschus

Manufacturer: Washington Homeopathic Products
Effective date: 2018-12-30
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:10:40

Label at a glance#

ProductAbelmoschus

Active ingredientABELMOSCHUS MOSCHATUS SEED

Label structure8 sections

Indications and uses

To relieve the symptoms of night fears.

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

ABELMOSCHUS

USES

OTC - PURPOSE SECTION

To relieve the symptoms of night fears.

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:

ABELMOSCHUS Night fears

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 ABELMOSCHUS is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Label

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
68428-000-07	2025-01-30	C162847	48780-1	2cef2736-7358-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-000-08	2025-01-30	C162847	48780-1	2cef2736-7358-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-000-09	2025-01-30	C162847	48780-1	2cef2736-7358-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-000-10	2025-01-30	C162847	48780-1	2cef2736-7358-d83d-e063-dadaa90ab31f	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68428-000-07	Abelmoschus	15 mL in 1 VIAL, GLASS	LIQUID	15	2
68428-000-08	Abelmoschus	30 mL in 1 VIAL, GLASS	LIQUID	30	2
68428-000-09	Abelmoschus	50 mL in 1 BOTTLE, GLASS	LIQUID	50	2
68428-000-10	Abelmoschus	100 mL in 1 BOTTLE, GLASS	LIQUID	100	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68428-000	ABELMOSCHUS (ABELMOSCHUS MOSCHATUS SEED) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS]	2	Legacy NDC, 4 package rows	20181231_84172f48-4825-4a22-b311-34db27d42078.zip

Products#

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

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

Abelmoschus
ABELMOSCHUS MOSCHATUS SEED
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68428-000	68428-000-07, 68428-000-08, 68428-000-09, 68428-000-10

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
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
ABELMOSCHUS MOSCHATUS SEED	UN2QZ55I88	ACTIB

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
7e3e9fce-f333-8cc9-e053-2a91aa0aad73			84172f48-4825-4a22-b311-34db27d42078	2018-12-30	Warnings	Exact identifier spl id: 7e3e9fce-f333-8cc9-e053-2a91aa0aad73 spl set id: 84172f48-4825-4a22-b311-34db27d42078

Reported adverse events (FAERS/openFDA)#

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