FDA.reportPublic FDA data

MYEVER

Manufacturer
Hubei Redrui Building Materials Co., Ltd. | Minyan Mengmeng (xiamen) Trading Co., Ltd | Guangzhou Yishenghe Traditional Chinese Medicine Technology Co., Ltd.
Effective date
2026-03-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:51:33

Label at a glance#

ProductMYEVER
Active ingredientESTRIOL
Label structure11 sections

Indications and uses

Temporarily relieves external vulvar dryness Helps prevent and temporarily protects irritated skin.

Dosage and administration

Cleanse hands and the external vulvar area with a mild, soap-free cleanser and pat dry. Apply a pea-sized amount (approx. 0.3 g) to the fingertip. Gently apply and massage into the dry areas of the vulva in a circular motion until fully absorbed. After an initial treatment of 2-3 weeks, reduce frequency to a maintenance level (e.g., twice a week).

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Estriol 0.2%

Purpose(s)

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

  • Temporarily relieves external vulvar dryness
  • Helps prevent and temporarily protects irritated skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • If you are pregnant or breast-feeding.
  • On minors under 18 years of age.
  • If you have a known sensitivity to estrogen or a hormone-related condition (e.g., breast cancer, endometriosis).
  • On open wounds, swollen areas, rashes, or active infections.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • A burning sensation, itching, or redness occurs and persists.
  • Condition worsens or symptoms last more than 7 days.

Pregnancy or breast feeding section

OTC - PREGNANCY OR BREAST FEEDING SECTION

Do not use if pregnant or breast-feeding.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  1. Cleanse hands and the external vulvar area with a mild, soap-free cleanser and pat dry.
  2. Apply a pea-sized amount (approx. 0.3 g) to the fingertip.
  3. Gently apply and massage into the dry areas of the vulva in a circular motion until fully absorbed.
  4. After an initial treatment of 2-3 weeks, reduce frequency to a maintenance level (e.g., twice a week).

Other information

OTHER SAFETY INFORMATION

  • Store in a cool, dry place below 25°C (77°F).
  • Avoid direct sunlight and high humidity.
  • Use within 6 months after opening.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, BUTYLENE GLYCOL, GLYCERIN, VITIS VINIFERA (GRAPE) SEED OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, SQUALANE, COCO-GLUCOSIDE, TOCOPHEROL, ASIATICOSIDE, SOY ISOFLAVONES, DIOSCOREA OPPOSITIFOLIA (WILD YAM) ROOT, POLYGONUM CUSPIDATUM ROOT, PUERARIA MONTANA VAR. LOBATA ROOT, HYALURONIC ACID, SODIUM HYALURONATE, SODIUM BENZOATE, POTASSIUM SORBATE, CIMICIFUGA RACEMOSA ROOT, PUNICA GRANATUM FRUIT JUICE, TRIFOLIUM PRATENSE (CLOVER) FLOWER, CAMELLIA SINENSIS LEAF EXTRACT, PANAX GINSENG ROOT, AVENA SATIVA (OAT) KERNEL OIL, PALMITOYL PENTAPEPTIDE-4, PALMITOYL TRIPEPTIDE-1, PALMITOYL TETRAPEPTIDE-7, CITRUS BIOFLAVONOIDS, GLABRIDIN, GINKGO BILOBA LEAF, MYRICETIN, CRITHMUM MARITIMUM, ERYNGIUM MARITIMUM ROOT

Questions or comments?

OTC - QUESTIONS SECTION

934-935-7135 / Rangelcervel824@gmail.com

Box Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MYEVER INTIMATE ESTRIOL CREAM PackagePackage

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87066-5915-1MYEVER1 g in 1 CARTONCREAM12

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87066-591587066-5915-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 matching rows.

Name, UNII, Kind table
NameUNIIKind
AQUA059QF0KO0RIACT
AVENA SATIVA (OAT) KERNEL OIL3UVP41R77RIACT
PALMITOYL TRIPEPTIDE-1RV743D216MIACT
PALMITOYL TETRAPEPTIDE-7Q41S464P1RIACT
CITRUS BIOFLAVONOIDSBD70459I50IACT
SODIUM BENZOATEOJ245FE5EUIACT
ERYNGIUM MARITIMUM ROOTOSE7C1M67DIACT
VITIS VINIFERA (GRAPE) SEED OIL930MLC8XGGIACT
SOY ISOFLAVONES71B37NR06DIACT
CIMICIFUGA RACEMOSA ROOTK73E24S6X9IACT
ESTRIOLFB33469R8EACTIB
POLYGONUM CUSPIDATUM ROOT7TRV45YZF7IACT
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
CRITHMUM MARITIMUMJ7IHY79BKYIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PUNICA GRANATUM FRUIT JUICE99S671U9KBIACT
MYRICETIN76XC01FTOJIACT
DIOSCOREA OPPOSITIFOLIA (WILD YAM) ROOT29CIF30B1ZIACT
ASIATICOSIDEPKO39VY215IACT
HYALURONIC ACIDS270N0TRQYIACT
SODIUM HYALURONATEYSE9PPT4THIACT
PALMITOYL PENTAPEPTIDE-4KK181SM5JGIACT
TOCOPHEROLR0ZB2556P8IACT
GLABRIDINHOC5567T41IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
GINKGO BILOBA LEAF19FUJ2C58TIACT
PUERARIA MONTANA VAR. LOBATA ROOTPET93F4I3CIACT
GLYCERINPDC6A3C0OXIACT
COCO-GLUCOSIDEICS790225BIACT
TRIFOLIUM PRATENSE (CLOVER) FLOWER4JS0838828IACT
PANAX GINSENG ROOTCUQ3A77YXIIACT
SQUALANEGW89575KF9IACT
CAMELLIA SINENSIS LEAFW2ZU1RY8B0IACT

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
MYEVERESTRIOL CREAMHubei Redrui Building Materials Co., Ltd.3ed85485-a441-4c05-e063-6394a90afef52026-03-25WarningsExact identifier
ndc (package): 87066-5915-1
ndc (product): 87066-5915
ndc11 (package): 87066591501
spl id: 4de4ae83-bd2d-b31a-e063-6394a90a3e1a
spl set id: 3ed85485-a441-4c05-e063-6394a90afef5

Reported adverse events (FAERS/openFDA)#

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