Bengama -

Manufacturer
Genuine Drugs
Effective date
2018-10-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:57:08

Label at a glance#

ProductBengama - Tolnaftate
Active ingredientTOLNAFTATE
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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1 %

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 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

ATHLETE'S FOOT SPRAY

COOL RELIEF

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 descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313421tolnaftate 1 % Topical SprayPSN1
313421tolnaftate 10 MG/ML Topical SpraySCD1
313421tolnaftate 1 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69666-833-042021-01-29C16284748780-1ba0f9c33-23c0-a910-e053-dadaa90a0b85Bengama-TOLNAFTATE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69666-833-04Bengama -Tolnaftate1 in 1 BOXAEROSOL, SPRAY11
69666-833-04Bengama -Tolnaftate128 g in 1 CANAEROSOL, SPRAY1281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69666-833BENGAMA - TOLNAFTATE (TOLNAFTATE) AEROSOL, SPRAY [GENUINE DRUGS]1Legacy NDC, 2 package rows20181103_0be7f384-4262-477f-9642-d6911dec5cbb.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69666-83369666-833-04

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
308e18c0-4a1c-4093-a1ce-1138d6c8a2fb0be7f384-4262-477f-9642-d6911dec5cbb2018-10-17WarningsExact identifier
spl id: 308e18c0-4a1c-4093-a1ce-1138d6c8a2fb
spl set id: 0be7f384-4262-477f-9642-d6911dec5cbb

Reported adverse events (FAERS/openFDA)#

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