Label: RITE AID MULTI-SYMPTOM RELIEF EYE DROPS- polyethylene glycol 400, tetrahydrozoline hcl, zinc sulfate solution/ drops
- NDC Code(s): 11822-0277-1
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 20, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purposes
- Uses
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Warnings
For external use only
When using this product
- pupils may become enlarged temporarily
- overuse may cause more eye redness
- remove contact lenses before using
- do not touch tip of container to any surface to avoid contamination
- replace cap after using
- do not use if this solution changes color or becomes cloudy
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Rite Aid Multi-Symptom Relief Eye Drops
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INGREDIENTS AND APPEARANCE
RITE AID MULTI-SYMPTOM RELIEF EYE DROPS
polyethylene glycol 400, tetrahydrozoline hcl, zinc sulfate solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0277 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC SULFATE 0.25 g in 100 mL POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL, UNSPECIFIED - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 400 1 g in 100 mL TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.05 g in 100 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) GLYCERIN (UNII: PDC6A3C0OX) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) WATER (UNII: 059QF0KO0R) BORIC ACID (UNII: R57ZHV85D4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0277-1 1 in 1 BOX 01/20/2023 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 01/20/2023 Labeler - Rite Aid Corporation (014578892) Registrant - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc. 174450460 manufacture(11822-0277) , pack(11822-0277) , label(11822-0277)