FDA.reportPublic FDA data

Abrotanum

Manufacturer
Washington Homeopathic Products
Effective date
2018-05-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:09:34

Label at a glance#

ProductAbrotanum
Active ingredientARTEMISIA ABROTANUM FLOWERING TOP
Label structure8 sections

Indications and uses

To relieve the symptoms of wrist pain.

Dosage and administration

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ABROTANUM   30C

USES

OTC - PURPOSE SECTION

To relieve the symptoms of wrist pain.

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:

ABROTANUMWrist pain

STOP USE AND ASK DOCTOR

WARNINGS SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The OTC potency range of ABROTANUM 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’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68428-173-032020-01-31C16284748780-19d75b9cf-ce2d-f424-e053-dadaa90a57ceDRUG FACTS
68428-173-052020-01-31C16284748780-19d75b9cf-ce2d-f424-e053-dadaa90a57ceDRUG FACTS
68428-173-062020-01-31C16284748780-19d75b9cf-ce2d-f424-e053-dadaa90a57ceDRUG FACTS
68428-173-112020-01-31C16284748780-19d75b9cf-ce2d-f424-e053-dadaa90a57ceDRUG FACTS
68428-173-122020-01-31C16284748780-19d75b9cf-ce2d-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68428-173-03Abrotanum75 in 1 VIAL, GLASSPELLET752
68428-173-05Abrotanum150 in 1 VIAL, GLASSPELLET1502
68428-173-06Abrotanum1200 in 1 BOTTLE, GLASSPELLET12002
68428-173-11Abrotanum300 in 1 BOTTLE, GLASSPELLET3002
68428-173-12Abrotanum600 in 1 BOTTLE, GLASSPELLET6002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68428-173ABROTANUM (ARTEMISIA ABROTANUM FLOWERING TOP) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]2Legacy NDC, 5 package rows20180503_ece83e73-f1ae-4519-93b2-9efb950fb858.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
68428-17368428-173-03, 68428-173-05, 68428-173-11, 68428-173-12, 68428-173-06

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
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT
ARTEMISIA ABROTANUM FLOWERING TOPQG07G580U0ACTIB

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
6b1f3c4a-025b-c60b-e053-2a91aa0a67deece83e73-f1ae-4519-93b2-9efb950fb8582018-05-01WarningsExact identifier
spl id: 6b1f3c4a-025b-c60b-e053-2a91aa0a67de
spl set id: ece83e73-f1ae-4519-93b2-9efb950fb858

Reported adverse events (FAERS/openFDA)#

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