Label: CLEAR EYES COMPLETE 7 SYMPTON RELIEF- hypromellose, naphazoline hydrochloride, polysorbate 80 and zinc sulfate liquid
- NDC Code(s): 67172-707-01
- Packager: Prestige Brands Holdings, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 25, 2024
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Warnings
For external use only.
When using this product:
- To avoid contamination, do not touch tip of container to any surface.
- Replace cap after using.
- Overuse of this product may produce increased redness of the eye.
- Pupils may become enlarged temporarily.
- To avoid contamination, do not touch tip of container to any surface.
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INGREDIENTS AND APPEARANCE
CLEAR EYES COMPLETE 7 SYMPTON RELIEF
hypromellose, naphazoline hydrochloride, polysorbate 80 and zinc sulfate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67172-707 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPROMELLOSES (UNII: 3NXW29V3WO) (HYPROMELLOSES - UNII:3NXW29V3WO) HYPROMELLOSES .5 mg in 1 mL NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE .0625 mg in 1 mL POLYSORBATE 80 (UNII: 6OZP39ZG8H) (POLYSORBATE 80 - UNII:6OZP39ZG8H) POLYSORBATE 80 1.25 mg in 1 mL ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION .625 mg in 1 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) EDETATE DISODIUM (UNII: 7FLD91C86K) POTASSIUM CHLORIDE (UNII: 660YQ98I10) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67172-707-01 1 in 1 BOX 06/12/2013 1 15 mL in 1 BOTTLE, DROPPER; 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 06/12/2013 Labeler - Prestige Brands Holdings, Inc. (159655021)