Bengama -

Manufacturer: Genuine Drugs
Effective date: 2018-10-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:57:09

Label at a glance#

ProductBengama - MICONAZOLE

Active ingredientMICONAZOLE NITRATE

Label structure9 sections

Dosage and administration

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.

Contacts and useful links#

Websitewww.inhalant.org

www.inhalant.org

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

MICONAZOLE 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

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:

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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:

DOSAGE & ADMINISTRATION SECTION

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:

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
998533	miconazole nitrate 2 % Topical Spray	PSN	1
998533	miconazole nitrate 20 MG/ML Topical Spray	SCD	1
998533	miconazole nitrate 2 % Topical Spray	SY	1
998533	miconazole nitrate 3 GM in 150 GM Topical Spray	SY	1

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
MICONAZOLE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3a55f4fb-5aec-4c88-0ff7-4d608ad4866a	Product name	1	20140508
5b9a7965-36d2-8412-dcaf-f76a65411611	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69666-832-04	2021-01-29	C162847	48780-1	ba0f9c33-23c3-a910-e053-dadaa90a0b85	Bengama-MICONAZOLE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69666-832-04	Bengama -MICONAZOLE	128 g in 1 CAN	AEROSOL, SPRAY	128		1
69666-832-04	Bengama -MICONAZOLE	1 in 1 BOX	AEROSOL, SPRAY	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69666-832	BENGAMA - MICONAZOLE (MICONAZOLE NITRATE) AEROSOL, SPRAY [GENUINE DRUGS]	1	Legacy NDC, 2 package rows	20181103_8483bbe9-6d27-482f-9055-a7af277ba069.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Bengama - MICONAZOLE
Miconazole Nitrate
MICONAZOLE
PROPANE
ISOBUTANE
ALCOHOL
TALC

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69666-832	69666-832-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MICONAZOLE NITRATE	VW4H1CYW1K	ACTIB
PROPANE	T75W9911L6	IACT
ISOBUTANE	BXR49TP611	IACT
ALCOHOL	3K9958V90M	IACT
TALC	7SEV7J4R1U	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
61ce59a1-9c4e-4d28-b4c5-0e231ef2fdf4			8483bbe9-6d27-482f-9055-a7af277ba069	2018-10-16	Warnings	Exact identifier spl id: 61ce59a1-9c4e-4d28-b4c5-0e231ef2fdf4 spl set id: 8483bbe9-6d27-482f-9055-a7af277ba069

Reported adverse events (FAERS/openFDA)#

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