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 13 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Equate Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN	Walmart	443e214b-2680-79a9-e063-6294a90a68ba	2025-12-20	Warnings	Exact identifier application number: M018
Equate Redness and Dry Eye Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Walmart	44155cf8-6fd9-d16f-e063-6394a90ac731	2025-12-20	Warnings	Exact identifier application number: M018
Original Redness Reliever	TETRAHYDROLIZINE HCL	Walmart	4414f768-0c69-d041-e063-6294a90a5bd9	2025-12-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant	POLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOL	Walgreens	21dfe061-4538-2061-e063-6394a90a6e73	2025-12-19	Warnings	Exact identifier application number: M018
Artificial Tears	GLYCERIN	Geri-Care Pharmaceuticals, Corp	7cc437e3-bad9-59be-e053-2991aa0a1da3	2025-12-19	Warnings	Exact identifier application number: M018
Signature Care Eye Drops Redness and Dry Eye Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Better Living Brands LLC	901f3bbe-e1bb-4e44-879c-711e59813a7f	2025-12-19	Warnings	Exact identifier application number: M018
STYE RELIEF SERUM	CARBOXYMETHYLCELLULOSE SODIUM(CMC)	Guangzhou Shimei Cosmetics Co., Ltd.	45fa7962-b489-4613-e063-6394a90a59b0	2025-12-15	Warnings	Exact identifier application number: M018
Gentle Eyes Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	TRP Company	13f99af6-b7d8-a092-e063-6394a90a5daa	2025-12-15	Warnings	Exact identifier application number: M018
Artificial Tears	GLYCERIN	NuCare Pharmaceuticals,Inc.	97a3d8e2-b2c0-3f5d-e053-2a95a90ac49d	2025-12-15	Warnings	Exact identifier application number: M018
Eyelash Serum	EYELASH SERUM	FlexiGo Inc	4544adf7-bb24-cb10-e063-6294a90aa414	2025-12-06	Warnings	Exact identifier application number: M018
Redness Reliever, Circle K	TETRAHYDROZOLINE HYDROCHLORIDE LIQUID	Lil' Drug Store products, Inc.	44e95d70-f633-1e4e-e063-6294a90a9f21	2025-12-01	Warnings	Exact identifier application number: M018
Splash Pure PF	PROPYLENE GLYCOL	LABORATORIOS SOPHIA, S.A. DE C.V.	40ad7ae5-1f2a-e3b1-e063-6294a90a6f84	2025-11-26	Warnings	Exact identifier application number: M018
Eyewash Station Additive Concentrate	CHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOL	Niagara Pharmaceuticals Inc.	362a6b6d-862d-4322-87a8-5b3a07fbe174	2025-11-24	Warnings	Exact identifier application number: M018
Rain Daily Hydration and Comfort For Dry Eyes	GLYCERIN	Rain Eye Drops, LLC	31d7c204-fb74-fb28-e063-6294a90ab330	2025-11-23	Warnings	Exact identifier application number: M018
Eyewash Additive Concentrate	WATER AND PROPYLENE GLYCOL	Haws Corporation	dd168403-398c-41ff-b1df-d93e4ff39de3	2025-11-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Walgreen Company	a39864a3-2407-7b7e-e053-2a95a90ab92f	2025-11-19	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Walgreen Company	a39919d5-84db-05df-e053-2995a90ab1d2	2025-11-19	Warnings	Exact identifier application number: M018
Sodium Chloride	SODIUM CHLORIDE	Walgreen Company	d112a344-33cc-41d3-bae6-492631ebdba7	2025-11-19	Warnings	Exact identifier application number: M018
Eyesaline Eyewash Concentrate	PURIFIED WATER	Honeywell Safety Products USA, Inc.	3765c251-eb14-d60f-e063-6294a90a6a4d	2025-11-12	Warnings	Exact identifier application number: M018
Eyesaline Emergency Eyewash	PURIFIED WATER	Honeywell Safety Products USA, Inc.	37f244fd-c02f-e66a-e063-6394a90aed81	2025-11-12	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