REFRESH P.M.

Product NDC: 0023-0240
11-digit product format: 000230240
Labeler code: 0023
Product ID: 0023-0240_9e93a73f-478a-40fe-adca-9b1c30bce567
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: 1990-04-23
Substance: MINERAL OIL; PETROLATUM
Active strength: 425; 573 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	0023-0240	0023-0240-04	D	Discontinued by firm		2026-10-15
excluded package	package	0023-0240	0023-0240-21	D	Discontinued by firm		2026-10-15

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	0023-0240-21	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	0023-0240-04	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	0023-0240-21	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	0023-0240-04	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	0023-0240-21	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	0023-0240-04	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	0023-0240-21	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	0023-0240-04	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	0023-0240-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	0023-0240-04	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	0023-0240-21	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	0023-0240-04	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	0023-0240-21	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	0023-0240-04	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	0023-0240-21	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	0023-0240-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	0023-0240-21	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	0023-0240-04	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	0023-0240-21	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	0023-0240-04	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	0023-0240-21	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	0023-0240-04	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	0023-0240-21	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	0023-0240-04	`557ba5c1ecfa…`	`9c80585c8c6e…`

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 P.M.
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MINERAL OIL	425 mg/g
PETROLATUM	573 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
702008	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
24365d64-cd94-41cc-a7e1-033102d98114	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0023-0240-04	REFRESH P.M.	1 in 1 CARTON	OINTMENT	1	9
0023-0240-04	REFRESH P.M.	3.5 g in 1 TUBE	OINTMENT	3.5	9
0023-0240-21	REFRESH P.M.	1 in 1 CARTON	OINTMENT	1	9
0023-0240-21	REFRESH P.M.	3.5 g in 1 TUBE	OINTMENT	3.5	9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0023-0240-04	GM - Gram	0023-0240	936d6dc5-9398-41da-86c0-ba83881ea170	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
mineral oil	ACTIVE INGREDIENT	T5L8T28FGP	REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	3
petrolatum	ACTIVE INGREDIENT	4T6H12BN9U	REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	3
mineral oil	ACTIVE MOIETY	T5L8T28FGP	REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	3
petrolatum	ACTIVE MOIETY	4T6H12BN9U	REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	3
lanolin alcohols	INACTIVE INGREDIENT	884C3FA9HE	REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0023-0240	REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.]	8	Current NDC, Legacy NDC, 4 package rows	20240120_24365d64-cd94-41cc-a7e1-033102d98114.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 7 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Vis Guard Lubricant Eye Drops	POLYVINYL ALCOHOL 1.4%	Ulai Health LLC	e9b0ed39-60c8-1093-e053-2a95a90a705b	2026-01-13	Warnings	Exact identifier application number: M018
carboxymethylcellulose sodium	CARBOXYMETHYLCELLULOSE SODIUM	AvPAK	b4697319-438e-2ec8-e053-2a95a90abb56	2026-01-08	Warnings	Exact identifier application number: M018
carboxymethylcellulose sodium	CARBOXYMETHYLCELLULOSE SODIUM	AvPAK	b478a695-ded0-2e5f-e053-2995a90ac45e	2026-01-08	Warnings	Exact identifier application number: M018
Lubricant Eye Drops Solution	POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL	AvPAK	f5743b38-e3d2-a065-e053-2995a90a4b9a	2026-01-08	Warnings	Exact identifier application number: M018
Plus Rinse Emergency Eyewash	PURIFIED WATER	INNOVATIVE SAFETY SUPPLY INC.	b3f47d26-39e4-4aea-bb92-358def52b652	2026-01-08	Warnings	Exact identifier application number: M018
pH Neutral Emergency Eyewash	WATER	INNOVATIVE SAFETY SUPPLY INC.	29a1bd1e-d0dd-478f-e063-6394a90ab0aa	2026-01-08	Warnings	Exact identifier application number: M018
Polyvinyl Alcohol Eye Drops 1,4 % w/v	POLYVINYL ALCOHOL EYE DROPS 1,4 % W/V	Aurolab	e8e09719-6e06-612b-e053-2995a90a79fc	2026-01-08	Warnings	Exact identifier application number: M018
Aurovisc	HYPROMELLOSE OPHTHALMIC SOLUTION 2% W/V	Aurolab	e9100312-b105-50a6-e053-2a95a90ac31f	2026-01-08	Warnings	Exact identifier application number: M018
TheraTears Dry and Tired	CARBOXYMETHYLCELLULOSE SODIUM	MEDTECH PRODUCTS INC	02b70e2d-8159-4637-a282-9eac1468e786	2026-01-07	Warnings	Exact identifier application number: M018
VISTA Hypromellose Dry Eye Relief	HYPROMELLOSE	Red Wedding LLC	b2c4954c-ed53-778a-e053-2a95a90ae0d0	2026-01-01	Warnings	Exact identifier application number: M018
Colirio Ojo De Aguila Eye Drops	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Grandall Distributing Co., Inc.	31aa07e9-0cc9-2a77-e063-6394a90a4b9d	2025-12-31	Warnings	Exact identifier application number: M018
Value Health by Prodose Eye Drops	TETRAHYDROZOLINE HYDROCHLORIDE AND POLYETHYLENE GLYCOL 400	Prodose, Inc.	3fafa362-a8a6-3f91-e063-6394a90a98b3	2025-12-31	Warnings	Exact identifier application number: M018
Signature Care Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Better Living Brands LLC	6f1f4f58-3208-4b06-9afb-c4beeed09314	2025-12-30	Warnings	Exact identifier application number: M018
Target Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Target Corporation	6c449374-8847-4c4a-9073-1951ff31d404	2025-12-30	Warnings	Exact identifier application number: M018
Target Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Target Corporation	ddc15dac-fbd8-42fa-80db-79f49fc6b9eb	2025-12-30	Warnings	Exact identifier application number: M018
Nighttime Relief Lubricant	LIGHT MINERAL OIL, WHITE PETROLATUM	Amerisource Bergen Drug Corp.	fd6b2be8-7e00-3765-e053-6294a90a4061	2025-12-30	Warnings	Exact identifier application number: M018
Rugby Carboxymethylcellulose Sodium 0.5% Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Rugby Laboratories	fb84fc0b-9a62-812a-e053-6394a90aba0a	2025-12-30	Warnings	Exact identifier application number: M018
Rugby Polyvinyl Alcohol 1.4% Lubricating Eye Drops	POLYVINYL ALCOHOL	Rugby Laboratories	081673b2-5c74-1200-e063-6394a90ae363	2025-12-30	Warnings	Exact identifier application number: M018
Medi-First Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Unifirst First Aid Corporation	a4e651cc-adf0-af9e-e053-2995a90ace5a	2025-12-30	Warnings	Exact identifier application number: M018
Green Guard Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	UniFirst First Aid Corporation	c3f04fdb-9fc1-797d-e053-2995a90afe80	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
702008	mineral oil 42.5 % / petrolatum 57.3 % Ophthalmic Ointment	PSN	24365d64-cd94-41cc-a7e1-033102d98114	9
702008	mineral oil 0.425 MG/MG / petrolatum 0.573 MG/MG Ophthalmic Ointment	SCD	24365d64-cd94-41cc-a7e1-033102d98114	9
702008	mineral oil 42.5 % / petrolatum, white 57.3 % Ophthalmic Ointment	SY	24365d64-cd94-41cc-a7e1-033102d98114	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0023-0240-04	00023024004	1 TUBE in 1 CARTON (0023-0240-04) > 3.5 g in 1 TUBE	1 tube	1990-04-23	0000-00-00	No	No	Current
0023-0240-21	00023024021	1 TUBE in 1 CARTON (0023-0240-21) > 3.5 g in 1 TUBE	1 tube	1990-04-23	0000-00-00	No	No	Current