Label: ORIGINAL REDNESS RELIEVER- naphazoline hydrochloride and polyethylene glycol 300 solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 11822-3215-3 - Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 1, 2014
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- Active ingredients
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Warnings
When using this product
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- do not touch tip of container to any surface to avoid contamination
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- do not overuse as it may produce increased redness of the eye
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- pupils may become enlarged temporarily
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- remove contact lenses before using
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- replace cap after use
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- Inactive ingredients
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INGREDIENTS AND APPEARANCE
ORIGINAL REDNESS RELIEVER
naphazoline hydrochloride and polyethylene glycol 300 solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-3215 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE 0.1 mg in 1 mL POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) (POLYETHYLENE GLYCOL 300 - UNII:5655G9Y8AQ) POLYETHYLENE GLYCOL 300 2 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) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-3215-3 1 in 1 CARTON 1 15 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 09/13/2010 Labeler - Rite Aid Corporation (014578892) Registrant - Bausch & Lomb Incorporated (196603781) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 114406598 MANUFACTURE(11822-3215)