xtra
Generic: benzalkonium chloride
Labeler: my imports usa llcDrug Facts
Product Profile
Brand Name
xtra
Generic Name
benzalkonium chloride
Labeler
my imports usa llc
Dosage Form
SPRAY
Routes
Active Ingredients
benzalkonium chloride .13 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
51628-4439
Product ID
51628-4439_2fb7084c-c45d-3832-e063-6394a90a8b0c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2024-11-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516284439
Hyphenated Format
51628-4439
Supplemental Identifiers
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
xtra (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .13 g/100mL
Packaging
- 399 mL in 1 BOTTLE, SPRAY (51628-4439-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2fb7084c-c45d-3832-e063-6394a90a8b0c", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["27f4ff15-5480-8842-e063-6294a90ad35b"], "manufacturer_name": ["MY IMPORTS USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "399 mL in 1 BOTTLE, SPRAY (51628-4439-1)", "package_ndc": "51628-4439-1", "marketing_start_date": "20241127"}], "brand_name": "XTRA", "product_id": "51628-4439_2fb7084c-c45d-3832-e063-6394a90a8b0c", "dosage_form": "SPRAY", "product_ndc": "51628-4439", "generic_name": "Benzalkonium Chloride", "labeler_name": "MY IMPORTS USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "XTRA", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".13 g/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241127", "listing_expiration_date": "20261231"}