uline eyewash

Generic: eyewash

Labeler: uline.
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

water 465 mL/473mL

Manufacturer
Uline.

Identifiers & Regulatory

Product NDC 69790-010
Product ID 69790-010_14545fec-97fe-aed7-e063-6394a90a016d
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 69790010
Hyphenated Format 69790-010

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 (69790-010-16)
  • 946 mL in 1 BOTTLE, UNIT-DOSE (69790-010-32)
source: ndc

Packages (2)

69790-010-16 473 mL in 1 BOTTLE, UNIT-DOSE (69790-010-16) 69790-010-32 946 mL in 1 BOTTLE, UNIT-DOSE (69790-010-32)

Ingredients (1)

water (465 mL/473mL)

Linked Drug Pages (1)

ULINE Eyewash ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "14545fec-97fe-aed7-e063-6394a90a016d", "openfda": {"unii": ["059QF0KO0R"], "rxcui": ["1151101"], "spl_set_id": ["14545fc9-1fb4-befa-e063-6294a90a0474"], "manufacturer_name": ["Uline."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, UNIT-DOSE (69790-010-16)", "package_ndc": "69790-010-16", "marketing_start_date": "20240401"}, {"sample": false, "description": "946 mL in 1 BOTTLE, UNIT-DOSE (69790-010-32)", "package_ndc": "69790-010-32", "marketing_start_date": "20240401"}], "brand_name": "ULINE Eyewash", "product_id": "69790-010_14545fec-97fe-aed7-e063-6394a90a016d", "dosage_form": "SOLUTION", "product_ndc": "69790-010", "generic_name": "Eyewash", "labeler_name": "Uline.", "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"}