Label: CLEAR EYES MAXIMUM ITCHY EYE RELIEF- glycerin and naphazoline hydrochloride and zinc sulfate liquid
- NDC Code(s): 67172-999-01, 67172-999-06
- Packager: Prestige Brands Holdings, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated August 21, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- pupils may become enlarged temporarily
- overuse may produce increased redness of the eye
- remove contact lenses before using
- to avoid contamination, do not touch tip to any surface
- replace cap after using
- pupils may become enlarged temporarily
- Directions
- Other Information
- Inactive Ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEAR EYES MAXIMUM ITCHY EYE RELIEF
glycerin and naphazoline hydrochloride and zinc sulfate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67172-999 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2.5 mg in 1 mL NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE .12 mg in 1 mL ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC SULFATE 2.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BORIC ACID (UNII: R57ZHV85D4) EDETATE DISODIUM (UNII: 7FLD91C86K) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67172-999-01 1 in 1 BOX 03/15/2011 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:67172-999-06 1 in 1 CARTON 09/04/2018 2 6 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 03/15/2011 Labeler - Prestige Brands Holdings, Inc. (159655021)