mg dermaclean
Labeler: morgan gallacher inc.Drug Facts
Product Profile
Brand Name
mg dermaclean
Labeler
morgan gallacher inc.
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride .13 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
50241-014
Product ID
50241-014_da16e124-7b03-48f6-a245-c37b9b67fe14
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M
Listing Expiration
2026-12-31
Marketing Start
2019-01-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50241014
Hyphenated Format
50241-014
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
mg dermaclean (source: ndc)
Generic Name
n a (source: label)
Application Number
M (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .13 g/100g
Packaging
- 1 BOTTLE, PLASTIC in 1 BOX (50241-014-02) / 3756 g in 1 BOTTLE, PLASTIC (50241-014-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "da16e124-7b03-48f6-a245-c37b9b67fe14", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["ed3d983e-0a6e-4de4-832a-0020f7711011"], "manufacturer_name": ["Morgan Gallacher Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (50241-014-02) / 3756 g in 1 BOTTLE, PLASTIC (50241-014-01)", "package_ndc": "50241-014-02", "marketing_start_date": "20190125"}], "brand_name": "MG DermaClean", "product_id": "50241-014_da16e124-7b03-48f6-a245-c37b9b67fe14", "dosage_form": "LIQUID", "product_ndc": "50241-014", "labeler_name": "Morgan Gallacher Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MG DermaClean", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".13 g/100g"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190125", "listing_expiration_date": "20261231"}