FDA.reportPublic FDA data

Menopause Plus Moisture

Manufacturer
Hyland's | Standard Homeopathic Company | Merical, Inc
Effective date
2018-04-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:55:21

Label at a glance#

ProductMenopause Plus Moisture
Active ingredientATROPA BELLADONNA, ANEMONE PULSATILLA, SULFUR, BERBERIS VULGARIS ROOT BARK, CAULOPHYLLUM THALICTROIDES ROOT, BLACK COHOSH, GRAPHITE, DELPHINIUM STAPHISAGRIA SEED, LACHESIS MUTA VENOM, SEPIA OFFICINALIS JUICE
Label structure7 sections

Indications and uses

Temporarily relieves the symptoms of vaginal dryness and soreness, irritation, pain, burning with accompanying 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#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Belladonna 12X HPUS, Berberis Vulgaris 12X HPUS, Caulophyllum 12X HPUS, Cimicifuga Racemosa 12X HPUS, Graphites 12X HPUS, Lachesis 30X HPUS, Pulsatilla 12X HPUS, Sepia Officinalis 12X HPUS, Staphysagria 6X HPUS, Sulphur 12X HPUS.

Uses

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Temporarily relieves the symptoms of vaginal dryness and soreness, irritation, pain, burning with accompanying 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. • symptoms are accompanied by abnormal vaginal

discharge.

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 - 60 TABLET BOTTLE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DOCTOR

WISE

MENOPAUSE+

MOISTURE

Natural relief of

vaginal dryness,

hot flashes & night sweats

60 SUBLINGUAL TABLETS

label1label1

label2label2

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54973-335754973-3357-1, 54973-3357-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ATROPA BELLADONNAWQZ3G9PF0HACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
SULFUR70FD1KFU70ACTIB
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
CAULOPHYLLUM THALICTROIDES ROOTJTJ6HH6YEHACTIB
BLACK COHOSHK73E24S6X9ACTIB
GRAPHITE4QQN74LH4OACTIB
DELPHINIUM STAPHISAGRIA SEED00543AP1JVACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
ACACIA5C5403N26OIACT

Source Document#

Source XML · Source PDF

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
d44d16a9-f15f-580a-e053-2a95a90ad37a6ada47ad-08b1-2291-e053-2991aa0a8ad02021-12-29WarningsExact identifier
spl set id: 6ada47ad-08b1-2291-e053-2991aa0a8ad0

Reported adverse events (FAERS/openFDA)#

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