FDA.reportPublic FDA data

MG DermaSan

Product NDC
50241-259
11-digit product format
502410259
Labeler code
50241
Product ID
50241-259_e2af03cb-3b39-4082-883d-13c72fd5d27f
Type
HUMAN OTC DRUG
Nonproprietary name
N/A
Dosage form
LIQUID
Route
TOPICAL
Labeler
Morgan Gallacher Inc.
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-10-01
Substance
BENZALKONIUM CHLORIDE
Active strength
.1 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE.1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1038791Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
d4c0de39-8570-4a05-a5e3-3752545ed95fAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50241-259-01MG DermaSan3756 g in 1 BOTTLE, PLASTICLIQUID375612
50241-259-02MG DermaSan1 in 1 BOXLIQUID112

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W7MG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1
BENZALKONIUMACTIVE MOIETY7N6JUD5X6YMG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1
CETRIMONIUM CHLORIDEINACTIVE INGREDIENTUC9PE95IBPMG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPMG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1
DIHYDROXYETHYL COCAMINE OXIDEINACTIVE INGREDIENT8AR51R3BL5MG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1
GLYCERETH-17 COCOATEINACTIVE INGREDIENT3057VPT0KCMG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1
LAURTRIMONIUM CHLORIDEINACTIVE INGREDIENTA81MSI0FICMG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1
waterINACTIVE INGREDIENT059QF0KO0RMG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50241-259MG DERMASAN (N/A) LIQUID [MORGAN GALLACHER INC.]11Current NDC, Legacy NDC, 2 package rows20241215_d4c0de39-8570-4a05-a5e3-3752545ed95f.zip

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 6 of 6 · 111 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MAX relief juniorACETAMINOPHENATLANTIC BIOLOGICALS CORP.396903dc-ae2d-4bf4-b1fd-0017b84abef92024-02-28WarningsExact identifier
application number: M
MAX relief juniorACETAMINOPHENATLANTIC BIOLOGICALS CORP.44730cbd-5b98-49bd-b3b8-6fecb0ccd1532024-02-28WarningsExact identifier
application number: M
HYDROCORTISONEHYDROCORTISONE ACETATEHART Health779f945f-ab69-40de-8d86-ab76debc5c7c2024-02-16WarningsExact identifier
application number: M
First Aid and BurnBENZALKONIUM CHLORIDE, LIDOCAINEHART Healthf5746bba-9d7f-4691-b466-14985473bf142024-02-16WarningsExact identifier
application number: M
IBUPROFENIBUPROFENHART Health1c1374e1-890f-48ab-8f93-e84da9d5bf842024-01-25WarningsExact identifier
application number: M
Hand SanitizerANTISEPTIC GELHART Healthf07daf29-d0db-4cf8-8baf-d175c2b2ef502024-01-25WarningsExact identifier
application number: M
Hydrogen PeroxideHYDROGEN PEROXIDEHART Health0346a322-8f6e-405a-8d17-8bc6ce5105a32024-01-24WarningsExact identifier
application number: M
AlcoholISOPROPYL ALCOHOLNorMed441b915a-287f-4734-b4d9-730b3d95e04c2024-01-24WarningsExact identifier
application number: M
Sooth-a-StingBENZOCAINEHART Healthbd7229b6-813a-4149-bfe2-fe682f270ff42024-01-18WarningsExact identifier
application number: M
First AidBENZALKONIUM CHLORIDE, BENZOCAINEHART Healtha6d258ed-6d6d-42f0-9994-6c2c4c3d0f4a2024-01-18WarningsExact identifier
application number: M
TRIBIOTICBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEHART Healthd8f175f9-f526-4c73-a171-49309ca16cb02024-01-18Warnings, Adverse reactionsExact identifier
application number: M

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038791benzalkonium chloride 0.1 % Topical SolutionPSNd4c0de39-8570-4a05-a5e3-3752545ed95f12
1038791benzalkonium chloride 1 MG/ML Topical SolutionSCDd4c0de39-8570-4a05-a5e3-3752545ed95f12
1038791benzalkonium chloride 0.1 % Topical SolutionSYd4c0de39-8570-4a05-a5e3-3752545ed95f12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50241-259-01502410259013756 g in 1 BOTTLE, PLASTIC3756 gHistorical
50241-259-02502410259021 BOTTLE, PLASTIC in 1 BOX (50241-259-02) / 3756 g in 1 BOTTLE, PLASTIC (50241-259-01) 2018-10-010000-00-00NoNoCurrent