Label: EQUATE EYE DROPS- tetrahyrozoline hydrochloride liquid
- NDC Code(s): 67172-281-01, 67172-282-01
- Packager: Prestige Brands Holdings, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 25, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- 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 enlarged temporarily
- to avoid contamination, do not touch tip of container to any surface
- Directions
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
EQUATE EYE DROPS
tetrahyrozoline hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67172-282 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.5 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:67172-282-01 1 in 1 BOX 02/11/2013 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 02/11/2013 EQUATE EYE DROPS
tetrahyrozoline hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67172-281 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.5 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:67172-281-01 1 in 1 BOX 02/11/2013 1 30 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 02/11/2013 Labeler - Prestige Brands Holdings, Inc. (159655021)