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United States · US · US:50241-339_1fe4feed-fa93-403a-b759-a6b2d0274961
MG DermaFoam
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMorgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1150241339021 BOTTLE, PLASTIC in 1 BOX (50241-339-02) / 3.80564 kg in 1 BOTTLE, PLASTIC (50241-339-01)
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": "50241-339_1fe4feed-fa93-403a-b759-a6b2d0274961",
"productndc": "50241-339",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "MG DermaFoam",
"active_ingred_unit": "kg/100kg",
"application_number": "M",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzalkonium Chloride",
"start_marketing_date": "20180925",
"active_numerator_strength": "13"
}Related drugs
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