FDA.reportPublic FDA data

Aletris Cordial

Manufacturer
Warsan Homoeopathic
Effective date
2019-07-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:19:29

Label at a glance#

ProductAletris Cordial
Active ingredientCAULOPHYLLUM THALICTROIDES ROOT, BLACK COHOSH, FRAXINUS AMERICANA BARK, CHAMAELIRIUM LUTEUM ROOT, ALETRIS FARINOSA ROOT, ANEMONE PULSATILLA, VIBURNUM OPULUS BARK, ZANTHOXYLUM AMERICANUM BARK, SEPIA OFFICINALIS JUICE, SARACA INDICA BARK, HYDRASTIS CANADENSIS WHOLE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Stop use and ask doctor if symptoms worsen or persist longer than 7 days.

If pregnant or breast-feeding, ask health professional before use.

Do not use if tamper evident seal is missing or broken.

OTC - ACTIVE INGREDIENT SECTION

Aletris Farinosa 1X
Jonesia Asoca 1X
Caulophyllum 1X
Cimifuga Racemosa 1X
Fraxnius Americana 1X
Helonia Dioica 1X
Hydrastis Candensis 1X
Pulsatilla 1X
Viburnum Opulus 1X
Xanothoxylum
Sepia 1X

OTC - PURPOSE SECTION

Temporary relief from irregular, painful periods and other disorders including scanty flow, premature periods, delayed periods, premenstrual pain, absence of menstruation, bearing down pain.

INACTIVE INGREDIENT SECTION

Purified Water

Sorbitol

DOSAGE & ADMINISTRATION SECTION

Adults and adolecents 12 years and older: One tablespoon three times daily as needed.

Children under the age of 12: Consult doctor prior to use.

INDICATIONS & USAGE SECTION

Temporary relief from irregular, painful periods and other disorders including scanty flow, premature periods, delayed periods, premenstrual pain, absence of menstruation, bearing down pain.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

aletris cordial.jpgaletris cordial.jpg

WARNINGS AND PRECAUTIONS SECTION

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69008-200169008-2001-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SORBITOL506T60A25RIACT
CAULOPHYLLUM THALICTROIDES ROOTJTJ6HH6YEHACTIB
BLACK COHOSHK73E24S6X9ACTIB
FRAXINUS AMERICANA BARK0B24UR1O1SACTIB
CHAMAELIRIUM LUTEUM ROOTDQV54Y5H3UACTIB
ALETRIS FARINOSA ROOTO021JGR97XACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
VIBURNUM OPULUS BARKT1UG6H6805ACTIB
ZANTHOXYLUM AMERICANUM BARKA4KL1HMZ7TACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
SARACA INDICA BARK341ALE870WACTIB
HYDRASTIS CANADENSIS WHOLER763EBH88TACTIB

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
ab715a4d-20f3-b011-e053-2a95a90acde28cbd6029-2506-4d8f-e053-2a95a90a5b812020-07-27WarningsExact identifier
spl set id: 8cbd6029-2506-4d8f-e053-2a95a90a5b81

Reported adverse events (FAERS/openFDA)#

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