san x e2
Generic: benzalkonium chloride
Labeler: amerisan, llcDrug Facts
Product Profile
Brand Name
san x e2
Generic Name
benzalkonium chloride
Labeler
amerisan, llc
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride .12 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
69884-706
Product ID
69884-706_2965dbef-0591-4303-e063-6394a90aeddc
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2022-01-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69884706
Hyphenated Format
69884-706
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
san x e2 (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .12 g/100mL
Packaging
- 1250 mL in 1 BOTTLE (69884-706-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2965dbef-0591-4303-e063-6394a90aeddc", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1053188"], "spl_set_id": ["d6e2f275-4609-24e6-e053-2995a90a8dd3"], "manufacturer_name": ["Amerisan, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1250 mL in 1 BOTTLE (69884-706-06)", "package_ndc": "69884-706-06", "marketing_start_date": "20220131"}], "brand_name": "SAN X E2", "product_id": "69884-706_2965dbef-0591-4303-e063-6394a90aeddc", "dosage_form": "LIQUID", "product_ndc": "69884-706", "generic_name": "Benzalkonium chloride", "labeler_name": "Amerisan, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SAN X E2", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".12 g/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220131", "listing_expiration_date": "20261231"}