Label: ULINE EYEWASH- eyewash solution
- NDC Code(s): 69790-010-16, 69790-010-32
- Packager: Uline.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated March 23, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Warnings
- Use
- Stop use and ask a doctor if you have any of the following
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Questions?
- Dosage & Administration
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ULINE EYEWASH
eyewash solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69790-010 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 465 mL in 473 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69790-010-16 473 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product 04/01/2024 2 NDC:69790-010-32 946 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product 04/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA022305 04/01/2024 Labeler - Uline. (039612668) Establishment Name Address ID/FEI Business Operations Niagara Pharmaceuticals, Inc. 205477792 manufacture(69790-010)