NDC 42961-237-01 - Xpect Hydrocortisone

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 42961-237
Requested NDC: 42961-237-01
Package NDCs from labels: 42961-237-01, 42961-237-02, 42961-237-03, 42961-237-04
Manufacturer: Cintas Corporation | SAFETEC OF AMERICA, INC
Effective date: 2025-09-26
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Xpect Hydrocortisone - Cintas Corporation \| SAFETEC OF AMERICA, INC	Cintas Corporation \| SAFETEC OF AMERICA, INC	2025-09-26	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
42961-237-01	Xpect Hydrocortisone	0.9 g in 1 PACKET	CREAM	0.9	3
42961-237-02	Xpect Hydrocortisone	10 in 1 BOX	CREAM	10	3
42961-237-03	Xpect Hydrocortisone	20 in 1 BOX	CREAM	20	3
42961-237-04	Xpect Hydrocortisone	10 in 1 BAG	CREAM	10	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42961-237	XPECT HYDROCORTISONE (HYDROCORTISONE) CREAM [CINTAS CORPORATION]	2	Current NDC, 4 package rows	20241228_45ef9be4-54c4-4d85-966b-27708313ded4.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 329 of 329 · 6,562 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eagle Brand Medicated Oil Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	54e45d89-e8c3-6fc3-e063-6394a90aac4e	2015-06-15	Warnings	Exact identifier application number: M017
Instant Hand Sanitizer	ALCOHOL	Safetec of America, Inc.	f9e30645-491b-4f54-acfd-f863ee235607	2013-08-07	Warnings	Exact identifier unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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