Vogelxo 12.5 MG/ACTUAT Transdermal Gel Pump, 60 ACTUAT

RxCUI: 1596785
RxNorm name: Vogelxo 12.5 MG/ACTUAT Transdermal Gel Pump, 60 ACTUAT
Display name: Vogelxo 12.5 MG/ACTUAT Transdermal Gel Pump, 60 ACTUAT
Full name: Vogelxo 12.5 MG/ACTUAT Transdermal Gel Pump, 60 ACTUAT
Term type: SY
Status: DailyMed mapping
Updated: 2026-06-04 23:38:52

RxNav Current And Historical NDCs#

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UNII Substances#

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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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Vogelxo	TESTOSTERONE	Upsher-Smith Laboratories, LLC	2dd150f6-cdfd-4d51-8888-12b288f26262	2025-07-14	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 1596785

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set ID	RxNorm string	TTY	SPL version	Label	Effective
2dd150f6-cdfd-4d51-8888-12b288f26262	Vogelxo 12.5 MG/ACTUAT Transdermal Gel Pump, 60 ACTUAT	SY	13	These highlights do not include all the information needed to use VOGELXO safely and effectively. See full prescribing information for VOGELXO. VOGELXO ® (testosterone) gel, for topical use, CIII Initial U.S. Approval: 1953	20250714
2dd150f6-cdfd-4d51-8888-12b288f26262	Vogelxo 1 % (12.5 MG/ACTUAT) Transdermal Gel Pump, 60 ACTUAT	PSN	13	These highlights do not include all the information needed to use VOGELXO safely and effectively. See full prescribing information for VOGELXO. VOGELXO ® (testosterone) gel, for topical use, CIII Initial U.S. Approval: 1953	20250714
2dd150f6-cdfd-4d51-8888-12b288f26262	60 ACTUAT testosterone 12.5 MG/ACTUAT Topical Gel [Vogelxo]	SBD	13	These highlights do not include all the information needed to use VOGELXO safely and effectively. See full prescribing information for VOGELXO. VOGELXO ® (testosterone) gel, for topical use, CIII Initial U.S. Approval: 1953	20250714