Label: CLEAR EYES MAXIMUM REDNESS RELIEF- naphazoline hydrochloride and glycerin liquid
- NDC Code(s): 67172-696-01, 67172-696-02
- Packager: Prestige Brands Holdings, Inc.
- Category: HUMAN OTC DRUG LABEL
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 June 26, 2023
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- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Active ingredients
- Purpose
- Uses
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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 may produce increased redness of the eye
- pupils may become temporarily enlarged
- to avoid contamination, do not touch tip of container to any surface
- Directions
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEAR EYES MAXIMUM REDNESS RELIEF
naphazoline hydrochloride and glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67172-696 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE 0.3 mg in 1 mL GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 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 BORATE (UNII: 91MBZ8H3QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67172-696-01 1 in 1 CARTON 09/01/2010 1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:67172-696-02 1 in 1 CARTON 09/01/2010 2 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 09/01/2010 Labeler - Prestige Brands Holdings, Inc. (159655021)