uline eyewash

Generic: eyewash

Labeler: niagara pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name uline eyewash
Generic Name eyewash
Labeler niagara pharmaceuticals inc.
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

water 465 mL/473mL

Manufacturer
Niagara Pharmaceuticals Inc.

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
1151101
UNII
059QF0KO0R

Packaging Origin

Original Packager
true

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
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 465 mL/473mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, UNIT-DOSE (65785-125-01)
  • 946 mL in 1 BOTTLE, UNIT-DOSE (65785-125-02)
source: ndc

Packages (2)

Ingredients (1)

water (465 mL/473mL)

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"}