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
Drug Label Information
Updated September 20, 2024
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- 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 Drug M018 03/15/2016 Labeler - Bausch & Lomb Incorporated (196603781)



