MINIDROPS

Product NDC: 64108-212
11-digit product format: 641080212
Labeler code: 64108
Product ID: 64108-212_49f38ac7-54c3-3b87-e063-6294a90a65a5
Type: HUMAN OTC DRUG
Nonproprietary name: Lubricant eye drops
Dosage form: LIQUID
Route: OPHTHALMIC
Labeler: Optics Laboratory, Inc
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1991-04-01
Substance: POVIDONE, UNSPECIFIED; POLYVINYL ALCOHOL
Active strength: 6; 14 mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: MINIDROPS
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
POVIDONE, UNSPECIFIED	6 mg/mL
POLYVINYL ALCOHOL	14 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
FZ989GH94E	Internal UNII lookup
532B59J990	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
359969	Internal RxNorm lookup
1046287	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
c13c5f91-50df-471c-a7c9-1747a2ac1250	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
64108-212-12	2021-03-02	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-12	2021-03-02	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-13	2021-03-02	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-13	2021-03-02	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-65	2021-03-02	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-65	2021-03-02	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-12	2021-01-29	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-12	2021-01-29	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-13	2021-01-29	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-13	2021-01-29	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-65	2021-01-29	c13c5f91-50df-471c-a7c9-1747a2ac1250
64108-212-65	2021-01-29	c13c5f91-50df-471c-a7c9-1747a2ac1250

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
64108-212-10	MINIDROPS	0.5 mL in 1 VIAL, SINGLE-USE	LIQUID	0.5	9
64108-212-12	MINIDROPS	30 in 1 BOX	LIQUID	30	9
64108-212-13	MINIDROPS	5 in 1 BOX	LIQUID	5	9
64108-212-65	MINIDROPS	65 in 1 BOX	LIQUID	65	9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
64108-212-12	EA - Each	64108-212	02c2830e-4730-414a-956e-31121c823bca	1	2015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
POLYVINYL ALCOHOL	ACTIVE INGREDIENT	532B59J990	MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC]	2
POVIDONE K30	ACTIVE INGREDIENT	U725QWY32X	MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC]	2
POLYVINYL ALCOHOL	ACTIVE MOIETY	532B59J990	MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC]	2
POVIDONE K30	ACTIVE MOIETY	U725QWY32X	MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC]	2
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64108-212	MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC]	7	Current NDC, Legacy NDC, 4 package rows	20241218_c13c5f91-50df-471c-a7c9-1747a2ac1250.zip

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 21 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Discount Drug Mart Redness Relief Eye Drops	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Discount Drug Mart, Inc.	31a98e6c-42df-6b56-e063-6294a90a3564	2024-01-01	Warnings	Exact identifier application number: M018
Harris Teeter Ultra Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Harris Teeter, LLC.	31ac6883-ffc6-39de-e063-6294a90a52dd	2024-01-01	Warnings	Exact identifier application number: M018
Exchange Select High Performance Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Army and Air Force Exchange Service	31ac8bd2-c2e9-6f2c-e063-6394a90adc72	2024-01-01	Warnings	Exact identifier application number: M018
CVS Health Fast Acting Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	CVS Pharmacy, Inc.	31addfd2-52f2-05b3-e063-6294a90a337f	2024-01-01	Warnings	Exact identifier application number: M018
Equate Eye Drops Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Wal-Mart Stores, Inc.	91fb8fb5-b871-4535-e053-2995a90a9b16	2023-12-23	Warnings	Exact identifier application number: M018
Equate Lubricant Eye Drops Preservative-Free	CARBOXYMETHYLCELLULOSE SODIUM	Wal-Mart Stores, Inc.	9228a39b-38d2-1dfc-e053-2a95a90a3c90	2023-12-23	Warnings	Exact identifier application number: M018
Equate Restore Plus Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Walmart, Inc.	9e665ca2-4fa6-fdb4-e053-2a95a90abcca	2023-12-23	Warnings	Exact identifier application number: M018
Sunmark Eye Drops Advanced Moisturizer/Lubricant	DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE	Strategic Sourcing Services LLC	0daa4e39-0447-44b6-a7d7-370b12bf9451	2023-12-23	Warnings	Exact identifier application number: M018
Equate Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Wal-Mart Stores, Inc.	91f85a72-5270-e4db-e053-2995a90aeb21	2023-12-23	Warnings	Exact identifier application number: M018
Equate Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Wal-Mart Stores, Inc.	e32233ef-ea15-45b8-8e83-b658cf4c56a0	2023-12-23	Warnings	Exact identifier application number: M018
Sunmark Eye Drops Original Formula	TETRAHYDROZOLINE HCL	Strategic Sourcing Services LLC	33efa7e9-4c3a-4d72-af31-c5e35095c2ff	2023-12-23	Warnings	Exact identifier application number: M018
Sunmark Lubricant Eye Drops	POLYPROPYLENE GLYCOL 400, PROPYLENE GLYCOL	Strategic Sourcing Services LLC	b117ff0a-1a48-4022-96e6-52bc45f056fc	2023-12-23	Warnings	Exact identifier application number: M018
Sunmark Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Strategic Sourcing Services LLC	043ccc34-44ee-416a-88bc-f247774e9075	2023-12-23	Warnings	Exact identifier application number: M018
Sunmark Lubricating Tears	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Strategic Sourcing Services LLC	58f0b6d7-6072-40fd-ba72-b3ed68834791	2023-12-23	Warnings	Exact identifier application number: M018
Leader Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Cardinal Health	8d9a4eec-bf0e-6c3b-e053-2995a90ae9aa	2023-12-23	Warnings	Exact identifier application number: M018
Leader Eye Wash	PURIFIED WATER	Cardinal Health	8d3ad11f-1945-f838-e053-2995a90a7aa5	2023-12-23	Warnings	Exact identifier application number: M018
Good Neighbor Pharmacy Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Amerisource Bergen Drug Corp.	fd2dc23f-6ccc-2644-e053-6294a90a889e	2023-12-23	Warnings	Exact identifier application number: M018
Rite Aid Eye Drops Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Rite Aid Corporation	fa1b5b66-9643-e9a7-e053-6394a90ae3cf	2023-12-23	Warnings	Exact identifier application number: M018
Signature Care Lubricant Eye Drops Long Lasting	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Better Living Brands, LLC	05a63929-fccd-2936-e063-6294a90aeac5	2023-12-23	Warnings	Exact identifier application number: M018
Meijer Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Meijer Distribution, Inc.	9feadde4-fbe5-0c9e-e053-2995a90a9b30	2023-12-22	Warnings	Exact identifier application number: M018

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
FZ989GH94E	POVIDONE, UNSPECIFIED	9003-39-8	POVIDONE, UNSPECIFIED

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1046287	MiniDrops 1.4 % / 0.6 % Ophthalmic Solution	PSN	c13c5f91-50df-471c-a7c9-1747a2ac1250	9
359969	polyvinyl alcohol 1.4 % / povidone 0.6 % Ophthalmic Solution	PSN	c13c5f91-50df-471c-a7c9-1747a2ac1250	9
1046287	polyvinyl alcohol 0.014 ML/ML / povidone 6 MG/ML Ophthalmic Solution [MiniDrops]	SBD	c13c5f91-50df-471c-a7c9-1747a2ac1250	9
359969	polyvinyl alcohol 0.014 ML/ML / povidone 6 MG/ML Ophthalmic Solution	SCD	c13c5f91-50df-471c-a7c9-1747a2ac1250	9
1046287	MiniDrops (polyvinyl alcohol 1.4 % / povidone 0.6 % ) Ophthalmic Solution	SY	c13c5f91-50df-471c-a7c9-1747a2ac1250	9
359969	polyvinyl alcohol 1.4 % / povidone 0.6 % Ophthalmic Solution	SY	c13c5f91-50df-471c-a7c9-1747a2ac1250	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
64108-212-10	64108021210	.5 mL in 1 VIAL, SINGLE-USE (64108-212-10)	1991-04-01		No	No	Current
64108-212-12	64108021212	30 VIAL, SINGLE-USE in 1 BOX (64108-212-12) / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10)	1991-04-01	0000-00-00	No	No	Current
64108-212-13	64108021213	5 VIAL, SINGLE-USE in 1 BOX (64108-212-13) / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10)	1991-04-01	0000-00-00	No	No	Current
64108-212-65	64108021265	65 VIAL, SINGLE-USE in 1 BOX (64108-212-65) / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10)	1991-04-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Lubricant eye drops - Optics Laboratory, Inc \| Taiwan Biotech	Optics Laboratory, Inc \| Taiwan Biotech	2026-02-03	HUMAN OTC DRUG LABEL	9