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United States · US · US:50241-259_e2af03cb-3b39-4082-883d-13c72fd5d27f
MG DermaSan
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMorgan Gallacher Inc.
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1150241259021 BOTTLE, PLASTIC in 1 BOX (50241-259-02) / 3756 g in 1 BOTTLE, PLASTIC (50241-259-01)
Annotations
UNII (FDA Substance ID)
F5UM2KM3W7
BENZALKONIUM CHLORIDE
RxCUI 1379
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F5UM2KM3W7",
"rxcui": "1379",
"inchikey": null,
"display_name": "BENZALKONIUM CHLORIDE",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"c5311836-674a-400b-a0d3-92f959d92682": {
"match": "brand_token",
"title": "MG FOAMSAN (BENZALKONIUM CHLORIDE) LIQUID [MORGAN GALLACHER INC. DBA CUSTOM CHEMICAL FORMULATORS INC.]",
"spl_version": "9",
"published_date": "2025-12-31"
}
},
"productid": "50241-259_e2af03cb-3b39-4082-883d-13c72fd5d27f",
"productndc": "50241-259",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "MG DermaSan",
"active_ingred_unit": "g/100g",
"application_number": "M",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "N/A",
"start_marketing_date": "20181001",
"active_numerator_strength": ".1"
}Related drugs
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