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Miracle GYN (4 Tablets)

Dosage form
TABLET
Labeler
Haudongchun Co., Ltd.
Label updated
2017-08-22
Retrieved
2026-09-07
Active ingredients
ALLANTOIN
View original label and images on DailyMed ↗
Active ingredient

Allantoin (11%)

Purpose

Vaginal skin protectant

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control right away. (1-800-222-1222)

Uses

- Relieves the following symptoms: vaginal irritation, itching and burning, odor, vaginal dryness

Warnings

For vaginal use only

Do not use if you have/are pregnat, hypersensitivity to any pain.

When using this product

- do not use during menstruation

- use clean underwear

- do not use tampons, douches, condoms, feminine clenasers, or other vaginal products

- do not eat or swallow

Stop use and ask a doctor if

- symptoms get worsen or do not get better

- symptoms last more than 7days

- you get rashes or hives, abdominal pain, fever, chillis, nausea, vomiting or foul-smelling vaginal odor or discharge

Store at room tmperature and in a dry place.

Directions

- Use it at bedtime preferably or during daytime without dynamic activites.

- Wash your finger and insert 2 pills into the vagina with first two knuckels of a finger. It will take 20-30 minutes until the pills are dissolved to relieve the symptoms and clean the vagina.

- Do not use within 6 hours prior to vaginal intercourse.

Dosage

- This product is for adults and children age of 4 and up.

- Use 2 tablets at a time 2-4 consecutive days until symptom are relieved.

- After then, keep using 2 tablets every week.

Inactive ingredients

Sodium Chloride, Soluble Collagen, Glucose, Magnesium Stearate, Aloe Barbadensis Leaf Extract, Cereus Grandiflorus (Cactus) Extract, Ginkgo Biloba Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Centella Asiatica Extract, Sophora Flavescens Root Extract, Angelica Gigas Root Extract

Miracle GYN (4 Tablets)

[Image in the official label — see DailyMed source]

DailyMed Set ID: 575bf24b-6074-7490-e053-2991aa0a1993 · Version 1
NDC: 55618-2008