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 11 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CareOne Maximum Redness Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCI	Retail Business Services, LLC	9ab96aed-21d3-11b6-e053-2995a90a7225	2025-12-30	Warnings	Exact identifier application number: M018
CVS Lubricant Eye Drops 30 ct	CARBOXYMETHYLCELLULOSE SODUIM	CVS Pharmacy, Inc.	8dbca077-c989-767a-e053-2995a90a7cf5	2025-12-30	Warnings	Exact identifier application number: M018
Foster and Thrive Original Formula Eye Drops	TETRAHYDROZOLINE HCL	Strategic Sourcing Services LLC	002da62b-aec6-8e2a-e063-6294a90a5efc	2025-12-30	Warnings	Exact identifier application number: M018
CareOne Artificial Tears Eye Drops 15mL	POLYVINYL ALCOHOL, POVIDONE	Retail Business Services, LLC	92fded6b-91fd-d82e-e053-2a95a90ab523	2025-12-30	Warnings	Exact identifier application number: M018
Foster and Thrive Long Lasting Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Strategic Sourcing Services LLC	00546df0-17d8-0e3c-e063-6294a90ae7b2	2025-12-30	Warnings	Exact identifier application number: M018
Meijer Multi-Symptom Relief	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE	Meijer, Inc.	e7a5677a-ff33-c039-e053-2a95a90ae6c7	2025-12-30	Warnings	Exact identifier application number: M018
TopCare Health Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Topcare Associates LLC	e8e9dfe5-3540-a4df-e053-2a95a90aaf98	2025-12-30	Warnings	Exact identifier application number: M018
Meijer Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Meijer Distribution, Inc.	b245f99f-785a-efdc-e053-2995a90a4911	2025-12-30	Warnings	Exact identifier application number: M018
Equate Original Eye Drops	TETRAHYDROZOLINE HCL	Walmart, Inc.	eb8e5beb-4454-58c2-e053-2a95a90a66e0	2025-12-30	Warnings	Exact identifier application number: M018
Avenova Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	NovaBay Pharmaceuticals, Inc.	cd17f037-5aa5-0ef8-e053-2a95a90a39cb	2025-12-30	Warnings	Exact identifier application number: M018
Equate Redness and Dry Eye Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCL	Wal-Mart Stores, Inc.	ae228018-9238-2cbd-e053-2995a90a8d99	2025-12-30	Warnings	Exact identifier application number: M018
Equate Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Walmart, Inc.	deebaf7f-f20d-4d7f-e053-2a95a90a4b4f	2025-12-30	Warnings	Exact identifier application number: M018
Quality Choice Artificial Tears Lubricant Eye Drops	POLYVINYL ALCOHOL, POVIDONE	Chain Drug Marketing Association, Inc.	1f669655-4bc7-0175-e063-6294a90a305a	2025-12-30	Warnings	Exact identifier application number: M018
Equate Artificial Tears	POLYVINYL ALCOHOL, POVIDONE	Walmart, Inc.	ead9f271-0f15-1fff-e053-2a95a90a93ac	2025-12-30	Warnings	Exact identifier application number: M018
Equate Multi-Symptom Relief Eye Drops	POLYETHYLENE GLYCOL 400,TETRAHYDROZOLINE HCL, ZINC SULFATE	Walmart, Inc.	eb8ed76b-9cd7-3636-e053-2a95a90a9583	2025-12-30	Warnings	Exact identifier application number: M018
CorneaCare Recover Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	CorneaCare Inc.	1fd3a5ed-8963-5c8e-e063-6394a90a6527	2025-12-30	Warnings	Exact identifier application number: M018
Eye Love Heyedrate Long Lasting Hydration	GLYCERIN, POVIDONE	Physician Recommended Neutraceuticals, L.P.	f321dea1-3251-eaa8-e053-2995a90aaf95	2025-12-30	Warnings	Exact identifier application number: M018
Quality Choice Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Chain Drug Marketing Assoc., Inc.	0cd1b36a-a07a-a1db-e063-6294a90a5994	2025-12-30	Warnings	Exact identifier application number: M018
Quality Choice Eye Drops Irritation Relief	TETRAHYDROZOLINE HCL, ZINC SULFATE	Quality Choice	1f682079-6e91-e14b-e063-6394a90a3f12	2025-12-30	Warnings	Exact identifier application number: M018
Quality Choice Moisturizing Relief Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	Chain Drug Marketing Association, Inc.	1fb81759-5931-59c8-e063-6294a90a2277	2025-12-30	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