Drop Dream Eye 2

Manufacturer: K&J.C Co., Ltd
Effective date: 2024-05-28
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:13:00

Label at a glance#

ProductDrop Dream Eye 2

Active ingredientPOLYAMINOPROPYL BIGUANIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

polyhexamethylene biguanide

INACTIVE INGREDIENT SECTION

poloxamer407, borax, oric acid, sodium hyaluronate, water, etc

OTC - PURPOSE SECTION

cleanses, rinses, disinfects, stores, lubricates and removed protein buildup

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

always use fresh solution to disinfacts, to not reuse solution

WARNINGS SECTION

keep in room temperature

DOSAGE & ADMINISTRATION SECTION

opthalmic use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52345-6001-1	2025-07-29	C162847	48780-1	3b156c62-2bb4-fb37-e063-e6dba90a4e07	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52345-6001-1	Drop Dream Eye 2	13 mL in 1 CONTAINER	LIQUID	13		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52345-6001	DROP DREAM EYE 2 (POLYHEXAMETHYLENE BIGUANIDE) LIQUID [K&J.C CO., LTD]	2	1 package rows	20240529_1706a2fb-1aa8-f084-e063-6294a90a9f26.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Drop Dream Eye 2
polyhexamethylene biguanide
POLYAMINOPROPYL BIGUANIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52345-6001	52345-6001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYAMINOPROPYL BIGUANIDE	DT9D8Z79ET	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
198116bc-d6d0-7a20-e063-6394a90ab2be			1706a2fb-1aa8-f084-e063-6294a90a9f26	2024-05-28	Warnings	Exact identifier spl id: 198116bc-d6d0-7a20-e063-6394a90ab2be spl set id: 1706a2fb-1aa8-f084-e063-6294a90a9f26

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.