Label: BLINK TEARS- polyethylene glycol 400 solution/ drops
- NDC Code(s): 40171-005-05, 40171-005-25, 40171-005-36
- 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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- OTC - ACTIVE INGREDIENT SECTION
- Purpose
- Uses
- WARNINGS
- Stop use and ask doctor if:
- OTC - KEEP OUT OF REACH OF CHILDREN SECTION
- Directions
- Other Information
- INACTIVE INGREDIENT SECTION
- OTC - QUESTIONS SECTION
- PRINCIPAL DISPLAY PANEL - 5 Vial Carton
- PRINCIPAL DISPLAY PANEL - 25 Vial Carton
-
PRINCIPAL DISPLAY PANEL - 180 Vial Carton
1 packer = 36 strips (180 vials)
Professional use - Not for resale
THIS SIDE UP
No. 94153
Store away from heat
Protect from freezingBlink® Tears Lubricating Eye Drops
0.01 fl oz (0.4 mL)
40171-00536Product of Germany
Blink is a trademark of
Johnson & Johnson
Surgical Vision, Inc.© Johnson & Johnson Surgical Vision, Inc. 2023
Johnson & Johnson Surgical Vision, Inc.
Irvine, CA 92618 U.S.A.
1-800-347-5005 -
INGREDIENTS AND APPEARANCE
BLINK TEARS
polyethylene glycol 400 solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:40171-005 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) Calcium Chloride (UNII: M4I0D6VV5M) Magnesium Chloride (UNII: 02F3473H9O) Potassium Chloride (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) Sodium Chloride (UNII: 451W47IQ8X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:40171-005-05 5 in 1 CARTON 03/15/2016 1 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product 2 NDC:40171-005-25 25 in 1 CARTON 03/15/2016 2 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product 3 NDC:40171-005-36 180 in 1 CARTON 03/23/2016 3 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 03/15/2016 Labeler - Bausch & Lomb Incorporated (196603781)