Petroleum

Product NDC: 53329-068
11-digit product format: 533290068
Labeler code: 53329
Product ID: 53329-068_40c14f0d-cd27-922b-e063-6394a90a375e
Type: HUMAN OTC DRUG
Nonproprietary name: White Petrolatum
Dosage form: JELLY
Route: TOPICAL
Labeler: Medline Industries, LP
Application: M016
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-01-01
Substance: PETROLATUM
Active strength: 1 g/g
NDC exclude flag: No
Listing certified through: 2026-12-31
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	53329-068	53329-068-04	D	Discontinued by firm		2026-10-15
excluded package	package	53329-068	53329-068-44	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	53329-068-44	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	53329-068-04	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	53329-068-44	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	53329-068-04	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	53329-068-44	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	53329-068-04	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	53329-068-44	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	53329-068-04	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	53329-068-44	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	53329-068-04	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	53329-068-44	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	53329-068-04	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	53329-068-44	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	53329-068-04	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	53329-068-44	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	53329-068-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	53329-068-04	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	53329-068-44	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	53329-068-44	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	53329-068-04	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	53329-068-44	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	53329-068-04	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	53329-068-44	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	53329-068-04	`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: Petroleum
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PETROLATUM	1 g/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
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
204754	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
34f3581f-39ba-4f28-9237-52f3820ab4c0	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
53329-068-01	2023-08-25	068 Curad Petroleum Jelly
53329-068-01	2023-08-25	068 Curad Petroleum Jelly
53329-068-04	2023-08-25	068 Curad Petroleum Jelly
53329-068-04	2023-08-25	068 Curad Petroleum Jelly
53329-068-16	2023-08-25	068 Curad Petroleum Jelly
53329-068-16	2023-08-25	068 Curad Petroleum Jelly
53329-068-44	2023-08-25	068 Curad Petroleum Jelly
53329-068-44	2023-08-25	068 Curad Petroleum Jelly
53329-068-96	2023-08-25	068 Curad Petroleum Jelly
53329-068-96	2023-08-25	068 Curad Petroleum Jelly
53329-068-01	2023-07-28	068 Curad Petroleum Jelly
53329-068-01	2023-07-28	068 Curad Petroleum Jelly
53329-068-04	2023-07-28	068 Curad Petroleum Jelly
53329-068-04	2023-07-28	068 Curad Petroleum Jelly
53329-068-16	2023-07-28	068 Curad Petroleum Jelly
53329-068-16	2023-07-28	068 Curad Petroleum Jelly
53329-068-44	2023-07-28	068 Curad Petroleum Jelly
53329-068-44	2023-07-28	068 Curad Petroleum Jelly
53329-068-96	2023-07-28	068 Curad Petroleum Jelly
53329-068-96	2023-07-28	068 Curad Petroleum Jelly

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
53329-068-01	Petroleum	28.4 g in 1 TUBE	JELLY	28.4	17
53329-068-01	Petroleum	1 in 1 BOX	JELLY	1	17
53329-068-04	Petroleum	118.29 g in 1 TUBE	JELLY	118.29	17
53329-068-16	Petroleum	5 g in 1 PACKET	JELLY	5	17
53329-068-44	Petroleum	113 g in 1 TUBE	JELLY	113	17
53329-068-96	Petroleum	144 in 1 CARTON	JELLY	144	17

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
53329-068-01	GM - Gram	53329-068	2519f4ed-7728-4e58-bf47-9f93cb91d3ba	1	2021-03-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
PETROLATUM	ACTIVE INGREDIENT	4T6H12BN9U	PETROLEUM (WHITE PETROLATUM) JELLY [MEDLINE INDUSTRIES, INC.]	7
PETROLATUM	ACTIVE MOIETY	4T6H12BN9U	PETROLEUM (WHITE PETROLATUM) JELLY [MEDLINE INDUSTRIES, INC.]	7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53329-068	PETROLEUM (WHITE PETROLATUM) JELLY [MEDLINE INDUSTRIES, LP]	16	Current NDC, Legacy NDC, 6 package rows	20250112_34f3581f-39ba-4f28-9237-52f3820ab4c0.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 21 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Daily Moisturizing	DIMETHICONE	Topco Associates LLC	47e54eee-70e0-4bfa-ae77-d61a6560a9e1	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL	Topco Associates LLC	471a9f8d-ba12-41d3-a510-20c1a13ff850	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Skin Protectant	PETROLATUM	Wakefern Food Corp.	b799229b-f7ca-494c-afde-1fd096aef66e	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Diaper Rash	ZINC OXIDE	WinCo Foods, LLC	659cc8c7-6300-41c0-a684-c5fde7f2b100	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M016
Zinc Oxide	ZINC OXIDE	Walgreen Co.	220f70e1-0802-4fe2-92d0-78dec557c993	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL	Walgreen Co.	417ae199-54bb-420f-a3cf-1c096062d78c	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M016
First Aid Beauty Dry Skin Rescue Kit	COLLOIDAL OATMEAL	The Procter & Gamble Manufacturing Company	4a93d029-d721-0bb5-e063-6294a90a17c4	2026-02-11	Warnings	Exact identifier application number: M016
Natouch Eczema Wipes	ECZEMA WIPES	Natouch LLC	0a9756a4-2fa9-cd19-e063-6294a90a93ad	2026-02-10	Warnings	Exact identifier application number: M016
EARTHS CARE Eczema Cream	ECZEMA	DLC Laboratories, Inc.	17436fa0-d6c7-1052-e063-6294a90adae4	2026-02-09	Warnings	Exact identifier application number: M016
Petrolatum	WHITE PETROLATUM	Retail Business Services, LLC	bf0c9494-0138-4346-9348-e235ca4d9e58	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M016
Clear Anti-Itch	PRAMOXINE HCL, ZINC ACETATE	Retail Business Services, LLC	a80b8fee-2dd9-4640-a4f8-4cf940df8563	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M016
Advanced Healing	PETROLATUM	Retail Business Services, LLC	6e9121c8-5eb9-4d0b-86c5-b892e14bdab8	2026-02-06	Warnings	Exact identifier application number: M016
Petrolatum	WHITE PETROLATUM	Retail Business Services, LLC	bf73c618-ed2f-4468-a51f-ff61c7b1f506	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M016
Daily Moisturizing	DIMETHICONE	Retail Business Services, LLC	c8a876e2-0a34-4c3d-a0bc-549dd3048e8a	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M016
Petroleum	WHITE PETROLATUM	Salado Sales Inc.	f973e3a5-3b45-4842-99ce-dff676ae1f96	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M016
Petroleum Skin Protectant	WHITE PETROLATUM	Pharmacy Value Alliance, LLC	0ce03cd1-c48d-45cf-b11f-08bade55dcb6	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M016
Daily Moisturizing	DIMETHICONE	Publix Super Markets, Inc.	28ac9de4-2a63-4839-bed5-9bcc59ebeb2a	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL	Publix Super Markets, Inc.	0098c983-c518-4a14-8635-c7bdde7bff4f	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M016
TN Dickinsons Pain and Itch Relief	PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE	Dickinson Brands Inc.	537c9c27-ee81-4920-8e3f-21edb844c9cf	2026-02-05	Warnings	Exact identifier application number: M016
Aveeno Eczema Therapy Nighttime Itch Relief Balm	COLLOIDAL OATMEAL	Kenvue Brands LLC	e3350a8f-b983-7c4d-e053-2a95a90a53f5	2026-02-04	Warnings	Exact identifier application number: M016

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4T6H12BN9U	PETROLATUM	8009-03-8	PETROLATUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
204754	petrolatum 100 % Topical Jelly	PSN	34f3581f-39ba-4f28-9237-52f3820ab4c0	17
204754	petrolatum 1 MG/MG Topical Ointment	SCD	34f3581f-39ba-4f28-9237-52f3820ab4c0	17
204754	petrolatum 100 % Topical Jelly	SY	34f3581f-39ba-4f28-9237-52f3820ab4c0	17

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53329-068-01	53329006801	1 TUBE in 1 BOX (53329-068-01) / 28.4 g in 1 TUBE	1 tube	2018-01-01	0000-00-00	No	No	Current
53329-068-04	53329006804	118.29 g in 1 TUBE (53329-068-04)	118.29 g	2019-02-21	0000-00-00	No	No	Current
53329-068-16	53329006816	5 g in 1 PACKET (53329-068-16)	5 g	2018-01-01	0000-00-00	No	No	Current
53329-068-44	53329006844	113 g in 1 TUBE (53329-068-44)	113 g	2018-01-01	2022-01-01	No	No	Current
53329-068-96	53329006896	144 PACKET in 1 CARTON (53329-068-96) / 5 g in 1 PACKET (53329-068-16)	144 packet	2018-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
068 Curad Petroleum Jelly	Medline Industries, LP	2025-10-09	HUMAN OTC DRUG LABEL	17
ST COVID-POD (Saliva Collection Kit) - Asclemed USA, Inc.	Asclemed USA, Inc.	2020-09-23	HUMAN PRESCRIPTION DRUG LABEL	1