tridergel
Generic: benzalkonium chloride
Labeler: trifluent pharma llcDrug Facts
Product Profile
Brand Name
tridergel
Generic Name
benzalkonium chloride
Labeler
trifluent pharma llc
Dosage Form
GEL
Routes
Active Ingredients
benzalkonium chloride .001 g/mL
Manufacturer
Identifiers & Regulatory
Product NDC
73352-520
Product ID
73352-520_baebaab7-5c13-426e-bcfb-4fdedb4885b4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2023-12-11
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73352520
Hyphenated Format
73352-520
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
tridergel (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .001 g/mL
Packaging
- 29.6 mL in 1 BOTTLE, WITH APPLICATOR (73352-520-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "baebaab7-5c13-426e-bcfb-4fdedb4885b4", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1049228", "2671305"], "spl_set_id": ["f12d9e8c-1d69-49d9-a9e9-a392c681aa6c"], "manufacturer_name": ["Trifluent Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29.6 mL in 1 BOTTLE, WITH APPLICATOR (73352-520-01)", "package_ndc": "73352-520-01", "marketing_start_date": "20231211"}], "brand_name": "Tridergel", "product_id": "73352-520_baebaab7-5c13-426e-bcfb-4fdedb4885b4", "dosage_form": "GEL", "product_ndc": "73352-520", "generic_name": "Benzalkonium Chloride", "labeler_name": "Trifluent Pharma LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tridergel", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".001 g/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231211", "listing_expiration_date": "20261231"}