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
- 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 April 20, 2023
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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 final part349 06/12/2013 Labeler - Prestige Brands Holdings, Inc. (159655021)