Label: LAGRIFILM PLUS- polyvinyl alcohol, and povidone solution/ drops
- NDC Code(s): 11980-165-15
- Packager: Allergan, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated February 11, 2020
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INGREDIENTS AND APPEARANCE
LAGRIFILM PLUS
polyvinyl alcohol, and povidone solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11980-165 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990) POLYVINYL ALCOHOL, UNSPECIFIED 14 mg in 1 mL POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E) POVIDONE, UNSPECIFIED 6.0 mg in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) 7.8 mg in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) CHLOROBUTANOL HEMIHYDRATE (UNII: 3X4P6271OX) 5.25 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11980-165-15 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/06/1968 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 01/06/1968 Labeler - Allergan, Inc. (144796497) Establishment Name Address ID/FEI Business Operations Allergan Sales, LLC 362898611 analysis(11980-165) , label(11980-165) , manufacture(11980-165) , pack(11980-165)
