Label: EYEWASH- purified water liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71271-100-01, 71271-100-02 - Packager: Reliance Medical Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 9, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Do not use
• if solution changes colour or becomes cloudy
• for injection
• as a contact lens solution.
When using the product
• do not re-use, once opened, discard.
• to avoid contamination, do not touch the tip of the container to any surface.
Stop use and consult a doctor if
• you experience eye pain.
• changes in vision.
• continued redness or irritation of the eye.
• the condition worsens or persists.
Obtain immediate medical treatment for all open wounds in or near the eyes.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredient
- Questions?
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
EYEWASH
purified water liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71271-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 0.991 mL 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:71271-100-01 25 in 1 CARTON 07/03/2017 1 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:71271-100-02 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/03/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 07/03/2017 Labeler - Reliance Medical Ltd (349044854)