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REFRESH REDNESS RELIEF - 0023-3414-15 - (phenylephrine hydrochloride, polyvinyl alcohol)

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Drug Information of REFRESH REDNESS RELIEF

Product NDC: 0023-3414
Proprietary Name: REFRESH REDNESS RELIEF
Non Proprietary Name: phenylephrine hydrochloride, polyvinyl alcohol
Active Ingredient(s): 1.2; 14    mg/mL; mg/mL & nbsp;   phenylephrine hydrochloride, polyvinyl alcohol
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of REFRESH REDNESS RELIEF

Product NDC: 0023-3414
Labeler Name: Allergan, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070514

Package Information of REFRESH REDNESS RELIEF

Package NDC: 0023-3414-15
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0023-3414-15) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of REFRESH REDNESS RELIEF

NDC Code 0023-3414-15
Proprietary Name REFRESH REDNESS RELIEF
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0023-3414-15) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 0023-3414
Product Type Name HUMAN OTC DRUG
Non Proprietary Name phenylephrine hydrochloride, polyvinyl alcohol
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20070514
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Allergan, Inc.
Substance Name PHENYLEPHRINE HYDROCHLORIDE; POLYVINYL ALCOHOL
Strength Number 1.2; 14
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of REFRESH REDNESS RELIEF


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