FDA.reportPublic FDA data

MG DermaFoam

Product NDC
50241-339
11-digit product format
502410339
Labeler code
50241
Product ID
50241-339_1fe4feed-fa93-403a-b759-a6b2d0274961
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-09-25
Substance
BENZALKONIUM CHLORIDE
Active strength
13 kg/100kg
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
MG DermaFoam
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE13 kg/100kg

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50241-339-01MG DermaFoam3.80564 kg in 1 BOTTLE, PLASTICLIQUID3.8056413
50241-339-02MG DermaFoam1 in 1 BOXLIQUID113

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50241-339MG DERMAFOAM (BENZALKONIUM CHLORIDE) LIQUID [MORGAN GALLACHER INC. DBA CUSTOM CHEMICAL FORMULATORS INC.]12Current NDC, Legacy NDC, 2 package rows20250212_4a43a605-f333-4c76-a476-476a9cc2e13a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50241-339-01502410339013.80564 kg in 1 BOTTLE, PLASTIC3.80564 kgHistorical
50241-339-02502410339021 BOTTLE, PLASTIC in 1 BOX (50241-339-02) / 3.80564 kg in 1 BOTTLE, PLASTIC (50241-339-01) 2018-09-250000-00-00NoNoCurrent