Label: BLINK TRIPLE CARE- polyethylene glycol 400 solution/ drops
- NDC Code(s): 29943-006-10, 29943-006-25
- Packager: Bausch & Lomb Incorporated
- 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 October 2, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
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Warnings
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- For external use only.
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- To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
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- Do not use if product changes color.
- Directions
- Inactive Ingredients
- Other Information
- PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
BLINK TRIPLE CARE
polyethylene glycol 400 solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:29943-006 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Polyethylene glycol 400 (UNII: B697894SGQ) (Polyethylene Glycol 400 - UNII:B697894SGQ) Polyethylene glycol 400 2.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength Boric Acid (UNII: R57ZHV85D4) Castor oil (UNII: D5340Y2I9G) Polyoxyl 40 hydrogenated castor oil (UNII: 7YC686GQ8F) Potassium chloride (UNII: 660YQ98I10) Water (UNII: 059QF0KO0R) Sodium borate (UNII: 91MBZ8H3QO) Sodium chloride (UNII: 451W47IQ8X) Sodium chlorite (UNII: G538EBV4VF) Hyaluronate sodium (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29943-006-10 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/01/2022 2 NDC:29943-006-25 2.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part349 05/01/2022 Labeler - Bausch & Lomb Incorporated (196603781)