Gyno-betadine
FDA Label NDC 72689-0042

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Oasis Trading for the product Gyno-betadine (NDC 72689-0042). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Purpose

Local treatment in the following cases: Candidate vaginitis, trichomonas vaginitis, non-specific and mixed infection, preoperative pre-operative treatment of obstetrics and gynecology, local cleaning and release

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Put 200 mg deep into the vagina once a day. It is advisable to insert it in the evening before bedtime. To increase or decrease appropriately according to age and symptoms.

Warnings

Do not use
in the eyes
as a first aid antiseptic longer than one week
on individuals who are allergic or sensitive to iodine
over large areas of the body
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredient

POLYETHYLENE GLYCOL 1540

Dosage & Administration

For vaginal use only

Package Label.Principal Display Panel

1 (212121)

1 (212121)

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