REFRESH LACRI-LUBE

Product NDC: 0023-0312
11-digit product format: 000230312
Labeler code: 0023
Product ID: 0023-0312_b6d64a52-8a8a-4c90-ac67-41a32cc3c78a
Type: HUMAN OTC DRUG
Nonproprietary name: mineral oil, petrolatum
Dosage form: OINTMENT
Route: OPHTHALMIC
Labeler: Allergan, Inc.
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1977-12-15
Substance: MINERAL OIL; PETROLATUM
Active strength: 425; 568 mg/g; mg/g
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: REFRESH LACRI-LUBE
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MINERAL OIL	425 mg/g
PETROLATUM	568 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
T5L8T28FGP	Internal UNII lookup
4T6H12BN9U	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
701984	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
d232a44b-516d-4cdf-a4e7-c3a9a50dc7af	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0023-0312-04	REFRESH LACRI-LUBE	1 in 1 CARTON	OINTMENT	1	8
0023-0312-04	REFRESH LACRI-LUBE	3.5 g in 1 TUBE	OINTMENT	3.5	8
0023-0312-07	REFRESH LACRI-LUBE	1 in 1 CARTON	OINTMENT	1	8
0023-0312-07	REFRESH LACRI-LUBE	7 g in 1 TUBE	OINTMENT	7	8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0023-0312-04	GM - Gram	0023-0312	20b39866-d70e-43a9-aba4-f2788fd84ed8	1	2012-07-24
0023-0312-07	GM - Gram	0023-0312	908fe98b-82bb-4d73-892c-9c93a24b96d6	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
mineral oil	ACTIVE INGREDIENT	T5L8T28FGP	REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	2
petrolatum	ACTIVE INGREDIENT	4T6H12BN9U	REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	2
mineral oil	ACTIVE MOIETY	T5L8T28FGP	REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	2
petrolatum	ACTIVE MOIETY	4T6H12BN9U	REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	2
chlorobutanol	INACTIVE INGREDIENT	HM4YQM8WRC	REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	2
lanolin alcohols	INACTIVE INGREDIENT	884C3FA9HE	REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	2
MINERAL OIL	ACTIVE INGREDIENT	T5L8T28FGP	MINERAL OIL (LACRI-LUBE) OINTMENT [REBEL DISTRIBUTORS CORP]	1
PETROLATUM	ACTIVE INGREDIENT	4T6H12BN9U	MINERAL OIL (LACRI-LUBE) OINTMENT [REBEL DISTRIBUTORS CORP]	1
MINERAL OIL	ACTIVE MOIETY	T5L8T28FGP	MINERAL OIL (LACRI-LUBE) OINTMENT [REBEL DISTRIBUTORS CORP]	1
PETROLATUM	ACTIVE MOIETY	4T6H12BN9U	MINERAL OIL (LACRI-LUBE) OINTMENT [REBEL DISTRIBUTORS CORP]	1
CHLOROBUTANOL	INACTIVE INGREDIENT	HM4YQM8WRC	MINERAL OIL (LACRI-LUBE) OINTMENT [REBEL DISTRIBUTORS CORP]	1
LANOLIN ALCOHOLS	INACTIVE INGREDIENT	884C3FA9HE	MINERAL OIL (LACRI-LUBE) OINTMENT [REBEL DISTRIBUTORS CORP]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0023-0312	REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	7	Current NDC, Legacy NDC, 4 package rows	20231215_d232a44b-516d-4cdf-a4e7-c3a9a50dc7af.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 9 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Medics Choice Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	K.C. Pharmaceuticals, Inc.	9ddfc275-602f-413b-e053-2995a90a11cb	2025-12-30	Warnings	Exact identifier application number: M018
Medics Choice Eye Drops Seasonal Relief	TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE	KC Pharmaceuticals, Inc.	92bd8cb4-90ad-4a47-afa4-30d1fa658d62	2025-12-30	Warnings	Exact identifier application number: M018
DG Health Advanced Relief Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	Dolgencorp LLC	9c62f8a3-7cf5-40f9-e053-2a95a90afd86	2025-12-30	Warnings	Exact identifier application number: M018
Medics Choice Eye Drops Original Redness Reliever	TETRAHYDROZOLINE HYDROCHLORIDE	KC Pharmaceuticals, Inc.	e42cb1bf-b985-4a1b-9a9b-ac27c2a5d7be	2025-12-30	Warnings	Exact identifier application number: M018
Medics Choice Eye Drops Maximum Redness Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	K.C. Pharmaceuticals, Inc.	f7131707-47af-d70a-e053-6394a90a418f	2025-12-30	Warnings	Exact identifier application number: M018
DG Original Eye Drops	TETRAHYDROZOLINE HCL	Dolgencorp LLC	9cb2123c-3ed4-ce8f-e053-2995a90a0ab8	2025-12-30	Warnings	Exact identifier application number: M018
Artificial Tears	POLYVINYL ALCOHOL, POVIDONE	KC Pharmaceuticals, Inc.	eb6eb6c4-1609-407b-84e4-c7509811f3c0	2025-12-30	Warnings	Exact identifier application number: M018
Medics Choice Eye Drops Advanced	TETRAHYDROZOLINE HYDROCHLORIDE, POLYETHYLENE GLYCOL 400, DEXTRAN 70, POVIDONE	KC Pharmaceuticals, Inc.	ab906fd8-265c-4359-a920-d626366e245c	2025-12-30	Warnings	Exact identifier application number: M018
Medics Choice Fresh and Soothe Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	KC Pharmaceuticals, Inc.	1f65b91a-4eac-65c2-e063-6394a90a0295	2025-12-30	Warnings	Exact identifier application number: M018
DG Health Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYPROPYLENE GLYCOL 400	Dolgencorp LLC	9cb20c3b-bf6d-8c7c-e053-2995a90aa485	2025-12-30	Warnings	Exact identifier application number: M018
DG Lubricant Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Dolgencorp LLC	9cb27899-6c36-3c37-e053-2995a90a1d43	2025-12-30	Warnings	Exact identifier application number: M018
Publix Artificial Tears Eye Drops	POLYVINYL ALCOHOL, POVIDONE	Publix Super Markets, Inc.	f5d1394b-0fe8-c372-e053-2a95a90a1f78	2025-12-30	Warnings	Exact identifier application number: M018
Best Choice Artificial Tears	POLYVINYL ALCOHOL, POVIDONE	Best Choice	f5ba63f3-7966-81fe-e053-2995a90a342c	2025-12-30	Warnings	Exact identifier application number: M018
DG Maximum Strength Redness Relief	GLYCERIN, NAPHAZOLINE HCL	Dolgencorp, Inc	9cb261ed-b708-1189-e053-2a95a90a547d	2025-12-30	Warnings	Exact identifier application number: M018
Publix Advanced Relief Eye Drops	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE	Publix Super Markets, Inc.	f7b0c3d6-0324-46c3-e053-6394a90a8241	2025-12-30	Warnings	Exact identifier application number: M018
Publix Moisturizing Relief Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Publix Super Markets, Inc.	9b391400-c53b-7c7b-e053-2995a90a2731	2025-12-30	Warnings	Exact identifier application number: M018
Publix High Performance Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Publix Super Markets, Inc.	9b402aa8-87cb-3928-e053-2995a90afa3c	2025-12-30	Warnings	Exact identifier application number: M018
Kroger Eye Drops Artificial Tears	POLYVINYL ALCOHOL, POVIDONE	The Kroger Company	f76f08c5-0111-8bc5-e053-6294a90a16ee	2025-12-30	Warnings	Exact identifier application number: M018
Health Mart Lubricating Tears	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Strategic Sourcing Services LLC	c8be678f-2b4a-4d39-9cb4-910d36d72174	2025-12-30	Warnings	Exact identifier application number: M018
Winco Maximum Redness Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCL	WinCo Foods, LLC	ff3651d4-42ce-4db1-a318-15f7592baf86	2025-12-30	Warnings	Exact identifier application number: M018

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
T5L8T28FGP	MINERAL OIL	8042-47-5	MINERAL OIL
4T6H12BN9U	PETROLATUM	8009-03-8	PETROLATUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
701984	mineral oil 42.5 % / petrolatum 56.8 % Ophthalmic Ointment	PSN	d232a44b-516d-4cdf-a4e7-c3a9a50dc7af	8
701984	mineral oil 0.425 MG/MG / petrolatum 0.568 MG/MG Ophthalmic Ointment	SCD	d232a44b-516d-4cdf-a4e7-c3a9a50dc7af	8
701984	mineral oil 42.5 % / petrolatum, white 56.8 % Ophthalmic Ointment	SY	d232a44b-516d-4cdf-a4e7-c3a9a50dc7af	8
701984	mineral oil 42.5 % / petrolatum 56.8 % Ophthalmic Ointment	PSN	3f0ec253-6179-4609-8a67-00dbefc55033	1
701984	mineral oil 0.425 MG/MG / petrolatum 0.568 MG/MG Ophthalmic Ointment	SCD	3f0ec253-6179-4609-8a67-00dbefc55033	1
701984	mineral oil 42.5 % / petrolatum, white 56.8 % Ophthalmic Ointment	SY	3f0ec253-6179-4609-8a67-00dbefc55033	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0023-0312-04	00023031204	1 TUBE in 1 CARTON (0023-0312-04) / 3.5 g in 1 TUBE	1 tube	1977-12-15	0000-00-00	No	No	Current
0023-0312-07	00023031207	1 TUBE in 1 CARTON (0023-0312-07) / 7 g in 1 TUBE	1 tube	1977-12-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
REFRESH ® LACRI-LUBE ® Drug Facts	Allergan, Inc.	2026-05-15	HUMAN OTC DRUG LABEL	8
Lacri-Lube Drug Facts	Rebel Distributors Corp	2011-02-17	HUMAN OTC DRUG LABEL	1