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 14 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
carboxymethylcellulose sodium	CARBOXYMETHYLCELLULOSE SODIUM	AvPAK	b479d2ae-4b59-916a-e053-2995a90af8ec	2025-11-11	Warnings	Exact identifier application number: M018
Sodium Chloride	SODIUM CHLORIDE	Rising Pharma Holdings, Inc.	42870188-b1d7-4934-a6c0-310530497dac	2025-11-07	Warnings	Exact identifier application number: M018
Systane Complete PF	PROPYLENE GLYCOL EMULSION	Alcon Laboratories, Inc.	798ffdde-1dba-4a3f-a0b6-937f9e958cca	2025-11-03	Warnings	Exact identifier application number: M018
LACRIFRESH HYDRAPF	GLYCERIN, POVIDONE	AVIZOR, S.A.	41bbd23e-0ec8-eb18-e063-6294a90a46d1	2025-10-27	Warnings	Exact identifier application number: M018
LACRIFRESH HYDRAMAXPF	GLYCERIN, POVIDONE	AVIZOR, S.A.	41be1604-89b4-7ec3-e063-6294a90a3331	2025-10-27	Warnings	Exact identifier application number: M018
Up and Up Dry Eye Relief Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Target Corporation	3b1834e6-75cf-5380-e063-6294a90ad1d5	2025-10-25	Warnings	Exact identifier application number: M018
Up and Up Dry Eye Relief Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Hanlim	420274c6-7bf0-0920-e063-6294a90a30be	2025-10-25	Warnings	Exact identifier application number: M018
Stye	POLYVINYL ALCOHOL AND POVIDONE	Medtech Products Inc.	60c11d3d-df20-4d1c-b425-49a84fecea30	2025-10-23	Warnings	Exact identifier application number: M018
TheraTears Lubricant	CARBOXYMETHYLCELLULOSE SODIUM	MEDTECH PRODUCTS INC	797b0394-2f0f-4733-8d20-ec5bdf3e085d	2025-10-23	Warnings	Exact identifier application number: M018
Advanced Eye Relief Dry Eye Rejuvenation	GLYCERIN PROPYLENE GLYCOL	Bausch & Lomb Incorporated	027969ee-64e4-4b08-bab7-c4cc8ed22f5f	2025-10-23	Warnings	Exact identifier application number: M018
TheraTears Lubricant	CARBOXYMETHYLCELLULOSE SODIUM	MEDTECH PRODUCTS INC	661d8764-8ae6-4229-9485-867553ee8e16	2025-10-23	Warnings	Exact identifier application number: M018
Refresh Relieva Preservative Free	CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN	Allergan, Inc.	3481f9b3-5a90-40d3-80f8-81f51cc864be	2025-10-22	Warnings	Exact identifier application number: M018
Sodium Chloride Normal Salt	SODIUM CHLORIDE	Method Pharmaceuticals	ce84727a-3677-4bf0-e053-2995a90a3ec8	2025-10-21	Warnings	Exact identifier application number: M018
iVIZIA Dry Eye	POVIDONE	Thea Pharma Inc.	1ef73cb1-da48-a713-e063-6294a90afa9d	2025-10-20	Warnings	Exact identifier application number: M018
Walgreens Ultra Lubricant	POLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOL	Walgreens	21dfe061-4533-2061-e063-6394a90a6e73	2025-10-17	Warnings	Exact identifier application number: M018
Walgreens	SODIUM CHLORIDE	Walgreen Company	21dfc2cf-65ae-c3fb-e063-6294a90a0a94	2025-10-17		Exact identifier application number: M018
Xpect Industrial Eye Relief	GLYCERIN, NAPHAZOLINE HCL	Cintas Corporation	a0167d06-7adb-36f4-e053-2a95a90af9ef	2025-09-30	Warnings	Exact identifier application number: M018
Xpect Eyewash	EYEWASH	Cintas Corporation	1d69365d-662b-4248-8fa9-1629451b549a	2025-09-30	Warnings	Exact identifier application number: M018
REFRESH OPTIVE Drops	CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN	Allergan, Inc.	80275190-d717-40ea-905b-5c8fbe986eac	2025-09-15	Warnings	Exact identifier application number: M018
Refresh Relieva PF Xtra	CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN	Allergan, Inc.	b51b8a75-8faa-430f-8f7e-ee58d3d13f2e	2025-09-15	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