Label: VISTA HYPROMELLOSE DRY EYE RELIEF- hypromellose gel
- NDC Code(s): 77790-002-10
- Packager: Red Wedding LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 1, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and consult a physician if you experience any of the following:
- Keep out of reach of children.
-
Directions
- Twist cap counterclockwise to break the seal.
- Unscrew the cap completely. Remove and discard the seal ring.
- If you wear contacts refer to package insert for complete directions
- shake well before using
- install 1 or 2 drops in the affected eye(s) as needed
- close the bottle tightly after use to ensure the stability of the solution
- Other information
- Inactive ingredients
- Questions?
- VISTA GEL™ Hypromellose USP 0.3% Dry Eye Relief Lubricating Gel Eye Drops 10 ml
-
INGREDIENTS AND APPEARANCE
VISTA HYPROMELLOSE DRY EYE RELIEF
hypromellose gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77790-002 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPROMELLOSE 2910 (50 MPA.S) (UNII: 1IVH67816N) (HYPROMELLOSE 2910 (50 MPA.S) - UNII:1IVH67816N) HYPROMELLOSE 2910 (50 MPA.S) 0.3 g in 1 mL Inactive Ingredients Ingredient Name Strength POTASSIUM CHLORIDE (UNII: 660YQ98I10) BORIC ACID (UNII: R57ZHV85D4) WATER (UNII: 059QF0KO0R) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) SORBITOL (UNII: 506T60A25R) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77790-002-10 1 in 1 BOX 01/01/2024 1 10 mL in 1 BOTTLE, DISPENSING; 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 01/01/2024 Labeler - Red Wedding LLC (117181523) Establishment Name Address ID/FEI Business Operations Wizcure Pharmaa Pvt Ltd 871769521 manufacture(77790-002)