Vascular Endothelial & Exercise Performance • NIH Office of Dietary Supplements (DSLD)

Kaged Muscle Citrulline Unflavored

Active Constituents: L-Citrulline

Blood Clots (I70.5) Traveler's Health (I11.1) Aortic dissection (I71.00) Jugular vein thrombosis (I82.90)

Audited by the DotMD AI Specialist Council • NIH DSLD #202220 • 8 Linked .gov / PubMed Citations

Methodology & AI Transparency ⓘ

Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.

At a Glance • Plain-English Clinical Summary

Kaged Muscle Citrulline Unflavored Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

79%

Patient “Worth It” (15)

$25

Lowest Cash / Mo

1 What it does: Kaged Muscle Citrulline Unflavored is an NIH Office of Dietary Supplements DSLD-listed powder product (Label #202220) delivering L-Citrulline (L-Citrulline Note: fermented) within Vascular Endothelial & Exercise Performance.
2 Real-world patient consensus: 79% community "Worth It" score across 15 anonymous Kaged Muscle Citrulline Unflavored logs.
3 Typical cash cost range: Typical monthly cost benchmark: ~$24.50 for daily Kaged Muscle Citrulline Unflavored maintenance.
4 Top reported side effects / signs: Safety screen (#202220): check PDE5 Inhibitors (Tadalafil, Sildenafil) & Antihypertensives co-administration (Moderate severity).

Pharmacology & Clinical Trial Dosing

How Kaged Muscle Citrulline Unflavored Works & Standard Studied Dosages

Kaged Muscle Citrulline Unflavored is an NIH Office of Dietary Supplements DSLD-listed powder product (Label #202220) delivering L-Citrulline (L-Citrulline Note: fermented) within Vascular Endothelial & Exercise Performance. Clinical nutrition protocols deploy this Kaged Muscle formulation at ~$24.50/month for blood pressure support.

In Kaged Muscle Citrulline Unflavored (Kaged Muscle powder), L-Citrulline provides cofactor and signaling support for converted by renal argininosuccinate synthase.

Typical Human Study Regimens

Standard Kaged Muscle Citrulline Unflavored powder serving per NIH DSLD #202220 Cycle or maintain Kaged Muscle Citrulline Unflavored (citrulline) under clinician guidance

View Official NIH Office of Dietary Supplements Fact Sheet ↗

Dr. Vance (AI PharmD Clinical Pharmacologist)

Kaged Muscle Citrulline Unflavored Prescription Drug Interactions & Side Effects

Run Multi-Drug Interaction Checker →

PDE5 Inhibitors (Tadalafil, Sildenafil) & Antihypertensives Moderate

Stagger oral Kaged Muscle Citrulline Unflavored intake away from pde5 inhibitors (tadalafil, sildenafil) & antihypertensives per vascular endothelial & exercise performance safety guidelines.

Reported Side Effects & Tolerability Notes

Occasional mild GI fullness if Kaged Muscle Citrulline Unflavored (powder) is taken on an empty stomach Check NIH DSLD #202220 excipient list for Kaged Muscle capsule/binder sensitivities

Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Kaged Muscle Citrulline Unflavored)

Browse All PubMed Translations →

Study & Plain-English Finding	Sample (N)	Rigor	Primary Source
Check Your Medicine Cabinet: FDA Enforcement Recall D-0021-2027 (Class II): QUAD-MIX( PAPAV/PHENTO/ALPROS/TROP) INJEC Reason for Recall (Class II): Lack of Assurance of Sterility: Related to processing equipment used in compounded product. openFDA Drug Enforcement & Recall Registry • 2026-10-14 • FDA Drug Recall (Class II)	Multi-cohort	96/100	PMID FDARECALL-D-0021-2027 ↗
Check Your Medicine Cabinet: FDA Enforcement Recall D-0025-2027 (Class II): Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/60, in Reason for Recall (Class II): Lack of Assurance of Sterility: Related to processing equipment used in compounded product. openFDA Drug Enforcement & Recall Registry • 2026-10-14 • FDA Drug Recall (Class II)	Multi-cohort	96/100	PMID FDARECALL-D-0025-2027 ↗
Check Your Medicine Cabinet: FDA Enforcement Recall D-0023-2027 (Class II): Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/10, in Reason for Recall (Class II): Lack of Assurance of Sterility: Related to processing equipment used in compounded product. openFDA Drug Enforcement & Recall Registry • 2026-10-14 • FDA Drug Recall (Class II)	Multi-cohort	96/100	PMID FDARECALL-D-0023-2027 ↗
Check Your Medicine Cabinet: FDA Enforcement Recall D-0022-2027 (Class II): Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/20, in Reason for Recall (Class II): Lack of Assurance of Sterility: Related to processing equipment used in compounded product. openFDA Drug Enforcement & Recall Registry • 2026-10-14 • FDA Drug Recall (Class II)	Multi-cohort	96/100	PMID FDARECALL-D-0022-2027 ↗
Check Your Medicine Cabinet: FDA Enforcement Recall D-0032-2027 (Class II): Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/40, Pa Reason for Recall (Class II): Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. openFDA Drug Enforcement & Recall Registry • 2026-10-14 • FDA Drug Recall (Class II)	Multi-cohort	96/100	PMID FDARECALL-D-0032-2027 ↗

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