MYRRH WOMAN

Manufacturer
MIR BIOTECHNOLOGY
Effective date
2018-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:17

Label at a glance#

ProductMYRRH WOMAN
Active ingredientMENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

menthol

INACTIVE INGREDIENT SECTION

sodium sulfate, niacinamide, olive leaf, adenosine, etc

OTC - PURPOSE SECTION

Cold odor Trichomonas candida infection treatment

Lack of come secretion

Vaginal cold urinary incontinence

Insensitivity to orgasms

Dry, rub and scar of Y zone

Lack of vaginal elasticity

Menopausal hormone imbalance

Lack of libido

WARNINGS SECTION

1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight

2. Do not use on open wounds, eczema, and other irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight

4. Use as avoiding eye areas.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Wash the Y zone thoroughly, then put the Woman Essence in a pill and put it deeply into the vagina
After 7 days, it is steadily used for 2 ~ 3 days for 4 months.

DOSAGE & ADMINISTRATION SECTION

for vaginal use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72263-0002-12020-01-31C16284748780-19d75b9d0-24d9-f424-e053-dadaa90a57ce6acabf35-a426-bcb3-e053-2991aa0a6f38

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72263-0002-1MYRRH WOMAN4 g in 1 BOTTLEPILL41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72263-0002MYRRH WOMAN (MENTHOL) PILL [MIR BIOTECHNOLOGY]1Legacy NDC, 1 package rows20180427_6acabf35-a426-bcb3-e053-2991aa0a6f38.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
72263-000272263-0002-1

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
MENTHOLL7T10EIP3AACTIB
ADENOSINEK72T3FS567IACT
NIACINAMIDE25X51I8RD4IACT

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
6acabf35-a427-bcb3-e053-2991aa0a6f386acabf35-a426-bcb3-e053-2991aa0a6f382018-04-26WarningsExact identifier
spl id: 6acabf35-a427-bcb3-e053-2991aa0a6f38
spl set id: 6acabf35-a426-bcb3-e053-2991aa0a6f38

Reported adverse events (FAERS/openFDA)#

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