MYRRH WOMAN ESSENCE- alcohol liquid

MYRRH WOMAN ESSENCE by

Drug Labeling and Warnings

MYRRH WOMAN ESSENCE by is a Otc medication manufactured, distributed, or labeled by MIR BIOTECHNOLOGY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

alcohol

INACTIVE INGREDIENT

water, menthol, citric acid, etc

PURPOSE

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

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INDICATIONS & USAGE

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

for vaginal use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MYRRH WOMAN ESSENCE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72263-0001
Route of Administration	VAGINAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72263-0001-1	20 g in 1 TUBE; Type 0: Not a Combination Product	04/27/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/27/2018

Labeler - MIR BIOTECHNOLOGY (694203851)

Registrant - MIR BIOTECHNOLOGY (694203851)

Establishment
Name	Address	ID/FEI	Business Operations
MIR BIOTECHNOLOGY		694203851	manufacture(72263-0001)