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 3 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Visine Red Eye Total Comfort Multi-Symptom	TETRAHYDROZOLINE HYDROCHLORIDE, POLYETHYLENE GLYCOL 400, AND ZINC SULFATE, UNSPECIFIED FORM	Kenvue Brands LLC	5747edef-7a87-41d7-9594-6c78508b9ba2	2026-06-11	Warnings	Exact identifier application number: M018
Nano Eye Drop Serum	WATER. SORBITOL.1.2-HEXANEDIOL GLYCERIN HYALURONATESODIUM.	Shenzhen Yiyang Zhiting Technology Co., Ltd	539567d6-488a-9b01-e063-6394a90abece	2026-06-06	Warnings	Exact identifier application number: M018
REFRESH CELLUVISC	CARBOXYMETHYLCELLULOSE SODIUM	Allergan, Inc.	b32ed9e8-d091-4f16-b416-5a62cdfee49a	2026-06-05	Warnings	Exact identifier application number: M018
VitaPhyte Redness Reliever Lubricant Eye Drops	REDNESS RELIEVER LUBRICANT EYE DROPS	Guangzhou Liyan Cosmetics Technology Co., Ltd.	53d4e9b0-c9a0-797a-e063-6294a90ad0cf	2026-06-04	Warnings	Exact identifier application number: M018
Rohto Digi-Eye	HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE	The Mentholatum Company	5d6f37b9-b568-4cb6-92de-eb40779f3f8c	2026-06-03	Warnings	Exact identifier application number: M018
Visine Red Eye Hydrating Comfort Eye Drops	TETRAHYDROZOLINE HYDROCHLORIDE AND POLYETHYLENE GLYCOL 400	Savings Distributors LLC	558178eb-1eec-af0f-e063-6394a90afad9	2026-06-01	Warnings	Exact identifier application number: M018
C-More Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN	PROFOUND NUTRITION LIMITED	78f04ecb-da5e-468c-81fe-70f7c26b76c2	2026-06-01	Warnings	Exact identifier application number: M018
Peep Club	GLYCERIN	Peep Club Eyecare Corp.	513d1988-2827-28d8-e063-6294a90a8d1f	2026-05-28	Warnings	Exact identifier application number: M018
Blink Triple Care Preservative Free	POLYETHYLENE GLYCOL 400	Bausch & Lomb Incorporated	65e67990-78b7-4ce9-963b-6bed3a6bed07	2026-05-27	Warnings	Exact identifier application number: M018
Ripple	GLYCERIN, POVIDONE	CorneaCare Inc	3b5ba197-d501-681e-e063-6294a90aefb5	2026-05-24	Warnings	Exact identifier application number: M018
REFRESH LACRI-LUBE	MINERAL OIL, PETROLATUM	Allergan, Inc.	d232a44b-516d-4cdf-a4e7-c3a9a50dc7af	2026-05-15	Warnings	Exact identifier application number: M018 ndc (product): 0023-0312
blink tears	POLYETHYLENE GLYCOL 400	Bausch & Lomb Incorporated	f1d07347-086f-43b2-aa5f-910764fc666e	2026-05-13	Warnings	Exact identifier application number: M018
Systane Pro PF	PROPYLENE GLYCOL	Alcon Laboratories, Inc.	a12baf3d-f22b-4c9f-a4c8-4e0d09f6d6f1	2026-05-12	Warnings	Exact identifier application number: M018
Sodium Hyaluronate Eye Drops	SODIUM HYALURONATE	Guangzhou Hechuang Commercial Service Co.,Ltd.	5187d136-15c6-517b-e063-6294a90a811d	2026-05-11	Warnings	Exact identifier application number: M018
Splash Tears	HYPROMELLOSE	LABORATORIOS SOPHIA, S.A. DE C.V.	a58a8478-9cc5-aa39-e053-2995a90a347d	2026-05-08	Warnings	Exact identifier application number: M018
iVIZIA Lubricant Eye Gel	POVIDONE	Thea Pharma Inc.	1f06ca1a-5270-9a82-e063-6294a90aed64	2026-04-29	Warnings	Exact identifier application number: M018
GoodSense Eye Drops Advanced Relief Moisturizer	DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	Preferred PHarmaceuticals Inc.	011473a8-26d5-4661-b3c0-745f9b6aa1d8	2026-04-29	Warnings	Exact identifier application number: M018
REFRESH TEARS PF	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN	Allergan, Inc.	9e1cba7b-84ed-47f3-b19a-121992834350	2026-04-24	Warnings	Exact identifier application number: M018
Sodium Chloride	SODIUM CHLORIDE	Method Pharmaceuticals, LLC	4b08859e-65bd-8255-e063-6394a90af614	2026-04-23	Warnings	Exact identifier application number: M018
Pure Eyes Sterile Eyes	NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN	SAMSON PHARMACEUTICAL	c0234e82-211f-4731-ac48-12db13b16e8a	2026-04-21	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