Pain Relief Cream

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	72425-201	72425-201-02	I	Inactivated by FDA		2026-10-05

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

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72425-201-02	Pain Relief Cream	1 in 1 BOX	CREAM	1		4
72425-201-02	Pain Relief Cream	28 g in 1 TUBE	CREAM	28		4

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72425-201	PAIN RELIEF CREAM (MENTHOL) CREAM [SANAMAX PLUS LLC]	4	Legacy NDC, 2 package rows	20250101_fee161dc-5047-4b98-9edc-130facbc731d.zip

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
416982	menthol 1.25 % Topical Cream	PSN	fee161dc-5047-4b98-9edc-130facbc731d	4
416982	menthol 12.5 MG/ML Topical Cream	SCD	fee161dc-5047-4b98-9edc-130facbc731d	4
416982	menthol 1.25 % Topical Cream	SY	fee161dc-5047-4b98-9edc-130facbc731d	4

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72425-201-02	72425020102	1 TUBE in 1 BOX (72425-201-02) > 28 g in 1 TUBE	1 tube	2019-12-02	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SanaMax PLUS PAIN RELIEF CREAM	SanaMax Plus LLC \| Identipak, Inc.	2024-12-30	HUMAN OTC DRUG LABEL	4