Soothe and Cool Free Moisture Barrier

Product NDC: 53329-072
11-digit product format: 533290072
Labeler code: 53329
Product ID: 53329-072_e9b0c006-8e8d-c5e5-e053-2995a90adb16
Type: HUMAN OTC DRUG
Nonproprietary name: Petrolatum
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Medline Industries, LP
Application: M016
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2007-01-01
Marketing end: 0000-00-00
Substance: PETROLATUM
Active strength: 93 g/100g
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	53329-072		D	Discontinued by firm	2026-10-12
excluded package	package	53329-072	53329-072-16	D	Discontinued by firm	2026-10-12
excluded package	package	53329-072	53329-072-96	D	Discontinued by firm	2026-10-12

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 · 33 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	53329-072-16	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	53329-072-96	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	53329-072-16	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	53329-072-96	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	53329-072-16	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	53329-072-96	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	53329-072-16	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	53329-072-96	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	53329-072-16	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	53329-072-96	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	53329-072-16	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	53329-072-96	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	53329-072-16	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	53329-072-96	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	53329-072-16	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	53329-072-96	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	53329-072-16	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	53329-072-96	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	53329-072-16	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	53329-072-96	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	53329-072-16	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	53329-072-96	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
60c52429-fcef-eb54-2387-43bc9e4f296b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
53329-072-16	2024-07-30	072 Soothe and Cool® Moisture Barrier
53329-072-96	2024-07-30	072 Soothe and Cool® Moisture Barrier
53329-072-16	2024-01-30	072 Soothe and Cool® Moisture Barrier
53329-072-96	2024-01-30	072 Soothe and Cool® Moisture Barrier

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
53329-072-16	GM - Gram	53329-072	76058714-78ee-4305-9591-ce9a23f5aa37	1	2019-08-06
53329-072-96	GM - Gram	53329-072	a5d31cf3-2ac0-4059-9601-659e2a74d3dc	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
PETROLATUM	ACTIVE INGREDIENT	4T6H12BN9U	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1
PETROLATUM	ACTIVE MOIETY	4T6H12BN9U	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1
BENZETHONIUM CHLORIDE	INACTIVE INGREDIENT	PH41D05744	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1
CHOLECALCIFEROL	INACTIVE INGREDIENT	1C6V77QF41	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1
ISOPROPYL MYRISTATE	INACTIVE INGREDIENT	0RE8K4LNJS	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1
VITAMIN A PALMITATE	INACTIVE INGREDIENT	1D1K0N0VVC	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53329-072	SOOTHE AND COOL FREE MOISTURE BARRIER (PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, LP]	4	Legacy NDC	20220928_a143042d-5de5-4440-8750-2b56f3b817c6.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 35 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Witch Hazel	WITCH HAZEL	Meijer Distribution Inc	03f23b04-e7f7-49b7-e063-6294a90ad58a	2025-10-31	Warnings	Exact identifier application number: M016
Diaper Rash skin protectant	LANOLIN AND PETROLATUM	Universal Distribution Centre LLC	1852246a-6a1c-49ab-e063-6294a90a9048	2025-10-30	Warnings	Exact identifier application number: M016
FB HYDRATING HAND SANITIZER	FB HYDRATING HAND SANITIZER	FAMILY DOLLAR SERVICES, LLC	20b531c1-9ab0-5ff1-e063-6394a90a2975	2025-10-30	Warnings	Exact identifier application number: M016
FB HYDRATING HAND SANITIZER	FB HYDRATING HAND SANITIZER	FAMILY DOLLAR SERVICES, LLC	20b650bd-18fe-8696-e063-6394a90aa9a2	2025-10-30	Warnings	Exact identifier application number: M016
FB HYDRATING HAND SANITIZER	FB HYDRATING HAND SANITIZER	FAMILY DOLLAR SERVICES, LLC	20b5f354-3379-3d9f-e063-6294a90ae817	2025-10-30	Warnings	Exact identifier application number: M016
Boudreauxs	ZINC OXIDE	C.B. Fleet Company, Inc.	59d90652-a471-4f77-a3d5-88aad9dc9e13	2025-10-30	Warnings	Exact identifier application number: M016
CVS Cools Itch Fast	HYDROCORTISONE	CVS Pharmacy, Inc.	8a4544df-bbba-47d2-ada0-352757abc91f	2025-10-29	Warnings	Exact identifier application number: M016
Winco Maximum Strength Hydrocortisone	HYDROCORTISONE	WINCO FOODS, LLC	b1812ea3-78cc-607a-e053-2a95a90a0a10	2025-10-29	Warnings	Exact identifier application number: M016
Good Neighbor Pharmacy Skin Protectant	ZINC OXIDE	AMERISOURCE BERGEN	c28e63f1-34be-9206-e053-2995a90accf6	2025-10-29	Warnings	Exact identifier application number: M016
Remedy Nutrashield	DIMETHICONE	Medline Industries, LP	ed8a08a7-594c-46e2-b70f-b75b2960141f	2025-10-28	Warnings	Exact identifier application number: M016
American Red Cross Anti-Itch	HYDROCORTISONE 1.0%(W/W)	MY IMPORTS USA LLC	421da126-a1c4-54d7-e063-6394a90ac401	2025-10-27	Warnings	Exact identifier application number: M016
GeriGard	ZINC OXIDE	Geri-Gentle Corporation	05b67830-adc8-46b1-b0a0-a6cd2875e80c	2025-10-27	Warnings	Exact identifier application number: M016
Boudreauxs Butt Barrier	DIMETHICONE	C.B. Fleet Company, Inc.	06a5af4d-40dd-42a4-8368-4d6a772d1b3a	2025-10-27	Warnings	Exact identifier application number: M016
Boudreauxs Baby Shower Bundle	ZINC OXIDE	C.B. Fleet Company, Inc.	a289ed3c-3c7a-4eda-bf5e-139203d2e17e	2025-10-27	Warnings	Exact identifier application number: M016
WinCo Original Strength Anti-Itch	DIPHENHYDRAMINE HYDROCHLORIDE, AND ZINC ACETATE	WinCo Foods, LLC	ae74e163-ba1a-4d1e-aaeb-9976bd202674	2025-10-24	Warnings	Exact identifier application number: M016
Maximum Strength Moisture Barrier	PETROLATUM AND ZINC OXIDE	Derma Sciences Canada Inc.	41ee91c0-d196-cc0f-e063-6394a90a7b97	2025-10-24	Warnings	Exact identifier application number: M016
Tenderphor	SKIN PROTECTANT	GERI-GENTLE CORPORATION	e6763da3-cbd1-7a86-e053-2995a90a26c1	2025-10-23	Warnings	Exact identifier application number: M016
Boudreauxs	ZINC OXIDE	C.B. Fleet Company, Inc.	262278f6-7e4c-44ee-b40d-39662a239d73	2025-10-23	Warnings	Exact identifier application number: M016
American Red Cross Anti-Itch	HYDROCORTISONE 1.0%(W/W)	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	41b8cb00-a04e-52f0-e063-6294a90aabf7	2025-10-22	Warnings	Exact identifier application number: M016
WinCo Foods Hydrocortisone Cream Intensive Healing	HYDROCORTISONE	WINCO FOODS, LLC	ac4e0e24-9295-b83b-e053-2995a90a996f	2025-10-22	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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53329-072-16	53329007216	5 g in 1 PACKET (53329-072-16)	5 g	2007-01-01	0000-00-00	No	No	Current
53329-072-96	53329007296	144 PACKET in 1 CARTON (53329-072-96) > 5 g in 1 PACKET (53329-072-16)	144 packet	2007-01-01	0000-00-00	No	No	Current