BEILLOSO WOMEN ESTRIOL- micronized estriol 0.1% women estriol cream

Beilloso Women Estriol by

Drug Labeling and Warnings

Beilloso Women Estriol by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Micronized Estriol 0.1%

Purpose

Relieves Vaginal Dryness

Use

.Provides temporary relief from Intimate dryness and discomfort.Moisturizes and soothes theIntimate area.

Warnings

1.For lntimate use only,not for oral use.
2.The product should not be use(as a substitute for medicinesad medical devices.

Do not use

Do not use if you are pregnant,during menstruation, or breastfeeding.

When Using

lf this is the first time you are experiencing vaginal dryness or discomfort. consult your healthcare provider.

Stop Use

·you experience abdominal pain.fever, chills,nausea.vomiting of foul-smelling discharge.·symptoms worsen or do not
improve within 7 days.

Ask Doctor

·you experience abdominal pain.fever, chills,nausea.vomiting of foul-smelling discharge.·symptoms worsen or do not
improve within 7 days.

Keep Oot Of Reach Of Children

.Keep out of reach of children,This product is for adult use onlv.

Directions

.Dispense 2 pumps ofcream onto clean fingers. ·Smooth over the inner lips and perineum.(Not for internal use). ·Apply once or twice a day.apply once or twice a day,apply at bedtime while lying down. ·Wait 20 minutes for the cream to deeply absorb for maximum overnight benefit.

Other information

Store in a dry and cool place at 20°-25°C(68°F-77°F).

Inactive ingredients

Purified Water, Vegetable Glycerin, Aloe Vera Gel.Caprylic/Capric Triglyceride.Scleroc Acid， olive Oil.Coconut Oil.Shea Butter. Methylsulfonylmethane(MsM).Stearyl Alcohol,Isopyl Palmitate,Allantoin.Carbomer, Sodium Bicarbonate.Herbal Extract(Natural Preservative)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEILLOSO WOMEN ESTRIOL 
micronized estriol 0.1% women estriol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-137
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ESTRIOL (UNII: FB33469R8E) (ESTRIOL - UNII:FB33469R8E)	ESTRIOL	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
STEARIC ACID (UNII: 4ELV7Z65AP)
SHEA BUTTER (UNII: K49155WL9Y)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER (UNII: 0A5MM307FC)
ALLANTOIN (UNII: 344S277G0Z)
OLIVE OIL (UNII: 6UYK2W1W1E)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-137-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/10/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/10/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)