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 17 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eyesaline Eyewash Concentrate	PURIFIED WATER	Honeywell Safety Products, Inc.	2d90c8e8-f479-3535-e063-6394a90af122	2025-02-07	Warnings	Exact identifier application number: M018
Code Red Eye Drops Redness Relief	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL	4 Trees, LLC	0aa08018-cc2d-d947-e063-6394a90a914a	2025-02-07	Warnings	Exact identifier application number: M018
Tyson 2.0 Mike Red Eye Drops For Dry High Eyes	GLYCERIN, NAPHAZOLINE HCL	Jbrands Pharma L.L.C.	288e9c85-0562-89bf-e063-6394a90a110d	2025-02-07	Warnings	Exact identifier application number: M018
Sodium Chloride Normal Salt	SODIUM CHLORIDE	Citragen Pharmaceuticals Inc	aae783b2-18fe-69ca-e053-2a95a90a0800	2025-01-30	Warnings	Exact identifier application number: M018
Sodium Chloride Normal Salt	SODIUM CHLORIDE	Citragen Pharmaceuticals Inc	82c29f1d-a018-7483-e053-2a91aa0a8f7e	2025-01-30	Warnings	Exact identifier application number: M018
OASIS Tears Lubricant Eye	GLYCERIN	OASIS Medical, Inc.	00071697-4ac6-4962-8eee-388b8b52bd40	2025-01-22	Warnings	Exact identifier application number: M018
ImproVue Lubricant	HYPROMELLOSE 2208 (15000 MPA.S)	Oculus Surgical, Inc.	63b82129-4848-47c5-bf92-ec4b1a9e9974	2025-01-22	Warnings	Exact identifier application number: M018
VISCO SHIELD Lubricant	HYPROMELLOSE 2208 (15000 MPA.S)	OASIS Medical, Inc.	72d22610-d8ab-4f24-b304-8b013430a7d7	2025-01-22	Warnings	Exact identifier application number: M018
OASIS Tears Plus Preservative-Free Lubricant Eye	GLYCERIN	OASIS Medical, Inc.	ea931c0f-c61e-4771-84f1-0274b1c3e28e	2025-01-22	Warnings	Exact identifier application number: M018
Medics Choice Soothing Eye Wash	PURIFIED WATER	KC Pharmaceuticals, Inc.	10e49808-161e-f4ec-e063-6294a90a1775	2025-01-19	Warnings	Exact identifier application number: M018
Sodium Chloride Hypertonicity Ophthalmic Solution, 5%	SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5%	Reliable 1 Laboritories LLC	29175c17-223e-5e92-e063-6294a90a71d2	2025-01-15	Warnings	Exact identifier application number: M018
Lubricating Tears	CARBOXYMETHYLCELLULOSE SODIUM 0.5% SOLUTION	Reliable 1 Laboritories LLC	29023a57-eba3-4241-e063-6294a90a7048	2025-01-15	Warnings	Exact identifier application number: M018
Aurodone Povidone Iodine 5 % Opthalmic Solution	POVIDONE IODINE 5 % TOPICAL SOLUTION	Aurolab	f3444446-1dad-79ff-e053-2a95a90af411	2025-01-06	Warnings	Exact identifier application number: M018
Hypromellose Eye Drops 0.7%	HYPROMELLOSE EYE DROPS 0.7%	Aurolab	d35313d0-b190-5fb0-e053-2a95a90a5283	2025-01-02	Warnings	Exact identifier application number: M018
VISTA MEIBO TEARS Propylene Glycol 0.6% w/v Advanced Dry Eye Relief Lubricating Drops 10 ml	PROPYLENE GLYCOL	Red Wedding LLC	b2c2fd0f-b944-6b0b-e053-2995a90aa216	2025-01-01	Warnings	Exact identifier application number: M018
Rite Aid Hydration Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Rite Aid Corporation	ecac1351-e944-21da-e053-2995a90a6d34	2024-12-31	Warnings	Exact identifier application number: M018
Lubricant Eye PM	MINERAL OIL, WHITE PETROLATUM	Reliable 1 Laboratories LLC	baec8045-97fe-6f60-e053-2a95a90a050e	2024-12-31	Warnings	Exact identifier application number: M018
Lil Drug Store Eye Drops Redness Reliever	TETRAHYDROZOLINE HYDROCHLORIDE	Lil Drug Store Products, Inc	d2a47e98-a04c-47ec-aded-d1c894f040e2	2024-12-30	Warnings	Exact identifier application number: M018
Rain Renewal Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Rain Eye Drops, LLC	af7a5768-7d1d-3d93-e053-2a95a90a38f6	2024-12-29	Warnings	Exact identifier application number: M018
Glitch Advanced Relief Eye Drops	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL	Misemer Pharmaceutical, Inc	03778509-3374-2168-e063-6294a90a9505	2024-12-23	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