Bengama -
FDA Label NDC 69666-832
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Genuine Drugs for the product Bengama - (NDC 69666-832). 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 drug facts, active ingredient, purpose, caution:, directions:, ingredients:, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
MICONAZOLE 2%
Purpose
Antifungal
Caution:
CONTENTS UNDER PRESSURE. Do not expose to heat or open flame, or store at temperatures above 120 °F (50°C). Do not spray near naked flame or incandescent material. Do not spray toward face. If eye contact occurs, rinse eyes well with water. If irritation persists, contact a physician. Do not intentionally inhale vapor or spray mist. Avoid contamination of food. Store in a cool dry space. Protect from direct sunlight. Dispose of container properly. Do not puncture or incinerate even when empty.
USE ONLY AS DIRECTED: Intentional misuse by deliberately concentrating and inhaling the contents can be harmful and fatal. Help stop inhalant abuse, for more information, visit www.inhalant.org
Directions:
SHAKE CAN WELL BEFORE EACH USE.
Hold about 6 inches away from feet. Spray generously on clean, dry feet and between toes. Use every day after bathing for results.
Ingredients:
Propellant, Ethanol, Talc, Fragrance.
Packaging
Image Description (Label 2)
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