Label: EQUATE REDNESS RELIEVER- tetrahydrozoline hydrochloride solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 79903-010-15, 79903-010-30 - Packager: WALMART INC.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 18, 2022
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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
- Questions?
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INGREDIENTS AND APPEARANCE
EQUATE REDNESS RELIEVER
tetrahydrozoline hydrochloride solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-010 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:79903-010-15 1 in 1 CARTON 04/26/2013 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:79903-010-30 1 in 1 CARTON 04/26/2013 2 30 mL in 1 BOTTLE; 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 04/26/2013 Labeler - WALMART INC. (051957769)