Label: DROP DREAM EYE 2- polyhexamethylene biguanide liquid
- NDC Code(s): 52345-6001-1
- Packager: K&J.C Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 26, 2024
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DROP DREAM EYE 2
polyhexamethylene biguanide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52345-6001 Route of Administration OPHTHALMIC, NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET) (POLYAMINOPROPYL BIGUANIDE - UNII:DT9D8Z79ET) POLYAMINOPROPYL BIGUANIDE 0.001 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52345-6001-1 13 mL in 1 CONTAINER; Type 0: Not a Combination Product 04/27/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/27/2024 Labeler - K&J.C Co., Ltd (690257639) Registrant - K&J.C Co., Ltd (690257639) Establishment Name Address ID/FEI Business Operations K&J.C Co., Ltd 690257639 manufacture(52345-6001)
