FDA.reportPublic FDA data

Menopause Plus Energy

Manufacturer
Hyland's Inc. | Merical, Inc
Effective date
2022-12-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:18:51

Label at a glance#

ProductMenopause Plus Energy
Active ingredientCAULOPHYLLUM THALICTROIDES ROOT, ATROPA BELLADONNA, SEPIA OFFICINALIS JUICE, ANEMONE PULSATILLA, LACHESIS MUTA VENOM, PHOSPHORIC ACID, BLACK COHOSH, DIBASIC POTASSIUM PHOSPHATE, SULFUR
Label structure7 sections

Indications and uses

Temporarily relieves the symptoms of fatigue, exhaustion, weakness, lack of focus, irritability, hot flashes, and night sweats experienced during menopause.

Dosage and administration

Adults: Take two tablets at onset of symptoms and repeat every four hours as needed.

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredients

Purpose

Belladonna 12X HPUS

hot flashes, night sweats

Caulophyllum 12X HPUS

irritability

Cimicifuga Racemosa 12X HPUS

hot flashes

Kali Phosphoricum 6X HPUS

exhaustion, weakness, fatigue

Lachesis 30X HPUS

hot flashes

Phosphoricum Acidum 12X HPUS

fatigue, weakness, lack of focus

Pulsatilla 12X HPUS

hot flashes, night sweats

Sepia Officinalis 12X HPUS

irritability, hot flashes, night sweats

Sulphur 12X HPUS

hot flashes, night sweats

“HPUS” indicates that the active ingredients are in the official Homeopathic Pharmacopœia of the United States.

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves the symptoms of fatigue, exhaustion, weakness, lack of focus, irritability, hot flashes, and night sweats experienced during menopause.

Warnings

WARNINGS SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

As with any drug, ask a doctor before use if pregnant or breast-feeding.

OTC - DO NOT USE SECTION

Do not use: • more than directed.  • if you have a known allergy to any ingredient in this product.

OTC - ASK DOCTOR SECTION

Consult a physician if symptoms persist for more than 7 days or worsen.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of reach of children. In case of accidental overdose, contact a medical professional or Poison Control Center immediately.

OTC - DO NOT USE SECTION

Do not use if imprinted tamper-evident bottle sleeve is broken or missing.

In case of emergency

SPL UNCLASSIFIED SECTION

In case of emergency, contact a medical professional or Poison Control Center immediately. Doctor Wise by Hyland’s may also be contacted for emergency information about our products 24 hours a day, 7 days per week at (800) 624-9659.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Take two tablets at onset of symptoms and repeat every four hours as needed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acacia Gum, Lactose

Questions or comments?

OTC - QUESTIONS SECTION

(800) 624-9659

Principal Display Panel - Doctor Wise Menopause plus Enerngy Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 54973-3354-1

DOCTOR

WISE

HOMEOPATHY

MENOPAUSE+

ENERGY

Natural relief of

fatigue, exhaustion,

hot flashes & night sweats*

SOY

FREE

68 SUBLINGUAL TABLETS

INCLUDES TWO 4-TABLET SACHETS

CartonCarton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54973-3354-12022-10-20C16284748780-1e4f33bdf-abba-d8a0-e053-dadaa90a6e4eDoctor Wise Menopause+ Energy
54973-3354-12022-07-29C16284748780-1e4f33bdf-abba-d8a0-e053-dadaa90a6e4eDoctor Wise Menopause+ Energy

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54973-3353MENOPAUSE PLUS ENERGY (CAULOPHYLLUM THALICTROIDES ROOT,DIBASIC POTASSIUM PHOSPHATE,PHOSPHORIC ACID,ANEMONE PULSATILLA,ATROPA BELLADONNA,BLACK COHOSH,LACHESIS MUTA VENOM,SULFUR AND SEPIA OFFICINALIS JUICE) KIT [HYLAND'S INC.]2Legacy NDC20221213_6a4f8662-2933-4bff-e053-2991aa0a3609.zip
54973-3354MENOPAUSE PLUS ENERGY (CAULOPHYLLUM THALICTROIDES ROOT,DIBASIC POTASSIUM PHOSPHATE,PHOSPHORIC ACID,ANEMONE PULSATILLA,ATROPA BELLADONNA,BLACK COHOSH,LACHESIS MUTA VENOM,SULFUR AND SEPIA OFFICINALIS JUICE) KIT [HYLAND'S INC.]2Legacy NDC20221213_6a4f8662-2933-4bff-e053-2991aa0a3609.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54973-335454973-3354-1
54973-335354973-3353-2, 54973-3353-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
ACACIA5C5403N26OIACT
CAULOPHYLLUM THALICTROIDES ROOTJTJ6HH6YEHACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
BLACK COHOSHK73E24S6X9ACTIB
DIBASIC POTASSIUM PHOSPHATECI71S98N1ZACTIB
SULFUR70FD1KFU70ACTIB
ACACIA5C5403N26OIACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
CAULOPHYLLUM THALICTROIDES ROOTJTJ6HH6YEHACTIB
DIBASIC POTASSIUM PHOSPHATECI71S98N1ZACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
BLACK COHOSHK73E24S6X9ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
SULFUR70FD1KFU70ACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB

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
413a733a-2d82-3f83-e063-6394a90a994b6a4f8662-2933-4bff-e053-2991aa0a36092025-10-15WarningsExact identifier
spl set id: 6a4f8662-2933-4bff-e053-2991aa0a3609

Reported adverse events (FAERS/openFDA)#

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