- INDICATIONS & USAGE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
WARNINGS
Warnings:
For external use only.
Do not use if: you experience any open wounds in or near the eye and obtain immediate medical treatment.
If solution changes color or becomes cloudy.
When using this product -To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard
Stop use and ask a doctor if you have any of the following: Changes in vision. Eye pain. Condition worsens or persists. Continued redness or irritation of the eye.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- PURPOSE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EYE WASH
purified water liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69103-2180 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 983 mg in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69103-2180-8 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/23/2015 2 NDC:69103-2180-7 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/23/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 07/23/2015 Labeler - Provision Medical Products (036936831) Registrant - Provision Medical Products (036936831)