BENGAMA - MICONAZOLE- miconazole nitrate aerosol, spray

Bengama - by

Drug Labeling and Warnings

Bengama - by is a Otc medication manufactured, distributed, or labeled by Genuine Drugs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

MICONAZOLE 2%

Purpose

Antifungal

INDICATIONS & USAGE

Foot Powder Spray instantly helps soothe, cool and comfort feet. Helps to absorb excess moisture a cause of athlete's foot. Use daily to help neutralize offensive foot odor.

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

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN THE USER OF THIS PRODUCT ASSUMES ALL RISKS OD USE STORAGE. AND HANDLING NOT IN ACCORDANCE WITH ITS DIRECTIONS AND CAUTIONS.

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.

SPL UNCLASSIFIED SECTION

MAXIMUM STRENGTH

ANTIFUNGAL SPRAY LIQUID

Cools And Soothes Athletes Foot

Fights Odor

Manufactured for

Genuine Drugs

P.O.Box: 362111 San Juan PR 00936

SEIN MENDEZ

Quality you can trust

MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

BENGAMA -  MICONAZOLE
miconazole nitrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69666-832
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PROPANE (UNII: T75W9911L6)
ISOBUTANE (UNII: BXR49TP611)
ALCOHOL (UNII: 3K9958V90M)
TALC (UNII: 7SEV7J4R1U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69666-832-04	1 in 1 BOX	11/01/2018
1		128 g in 1 CAN; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	11/01/2018

Labeler - Genuine Drugs (079610378)