uline eyewash
Generic: eyewash
Labeler: niagara pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
uline eyewash
Generic Name
eyewash
Labeler
niagara pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
water 465 mL/473mL
Manufacturer
Identifiers & Regulatory
Product NDC
65785-125
Product ID
65785-125_445cc5b0-291c-a344-e063-6394a90a0298
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA022305
Listing Expiration
2026-12-31
Marketing Start
2024-04-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65785125
Hyphenated Format
65785-125
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
uline eyewash (source: ndc)
Generic Name
eyewash (source: ndc)
Application Number
NDA022305 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 465 mL/473mL
Packaging
- 473 mL in 1 BOTTLE, UNIT-DOSE (65785-125-01)
- 946 mL in 1 BOTTLE, UNIT-DOSE (65785-125-02)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "445cc5b0-291c-a344-e063-6394a90a0298", "openfda": {"unii": ["059QF0KO0R"], "rxcui": ["1151101"], "spl_set_id": ["2d7f22d2-320b-6af1-e063-6294a90addc6"], "manufacturer_name": ["Niagara Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, UNIT-DOSE (65785-125-01)", "package_ndc": "65785-125-01", "marketing_start_date": "20240401"}, {"sample": false, "description": "946 mL in 1 BOTTLE, UNIT-DOSE (65785-125-02)", "package_ndc": "65785-125-02", "marketing_start_date": "20240401"}], "brand_name": "ULINE Eyewash", "product_id": "65785-125_445cc5b0-291c-a344-e063-6394a90a0298", "dosage_form": "SOLUTION", "product_ndc": "65785-125", "generic_name": "Eyewash", "labeler_name": "Niagara Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ULINE Eyewash", "active_ingredients": [{"name": "WATER", "strength": "465 mL/473mL"}], "application_number": "NDA022305", "marketing_category": "NDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}