RipFACTOR® (Sphaeranthus + Mango Bark Blend for Muscle Strength — PLT Health)

Sphaeranthus indicus / Mangifera indica
Evidence Level
Limited
2 Clinical Trials
4 Documented Benefits
2/5 Evidence Score

RipFACTOR® is a branded blend of Sphaeranthus indicus (East Indian globe thistle) flower head extract and Mangifera indica (mango tree) bark extract, developed by Laila Nutraceuticals and sold by PLT Health Solutions. It has been tested in two 8-week, placebo-controlled trials in young Indian men doing resistance training, 40 and 99 men, both funded by companies with a commercial interest in the ingredient. Both reported larger gains in bench press and leg strength than training with placebo, and higher free testosterone; in the larger trial, testosterone was not higher than in a placebo group doing twice the training. The strength gains in the smaller trial were unusually large for a supplement, the two parts of the blend have not been tested separately in people, and no independent group has published a replication. No women or men over 40 have been studied.

Studied Dose Tested: 650 mg/day of LI12542F6 for 56 days, or 425 or 850 mg/day of a water-dispersible version; the two were standardized differently, so equal mass is not an equal marker dose.
Active Compound Standardized 2:1 blend of Sphaeranthus indicus flower head extract and Mangifera indica bark extract.

Benefits

Muscle strength with resistance training

In 40 recreationally active men taking 650 mg/day for 8 weeks, bench press 1RM rose 27.6 kg vs 5.0 kg on placebo and leg press 29.5 kg vs 5.7 kg, unusually large gains for any supplement. In 99 previously untrained men, 850 mg/day added 13.8 kg on bench press over placebo with the same training. Both trials were small, single-site and industry-funded.

Strength compared with doubled training volume

In the 99-man trial, both doses lifted more than a placebo group doing two training sets on leg extension and total strength, and 850 mg/day did so on bench press (9.9 kg). However, the double-set placebo group never lifted significantly more than the single-set placebo group, so this comparison shows less than it seems.

Free and total testosterone levels in young men

In 99 young men with normal testosterone, 8 weeks of 850 mg/day raised total testosterone from 626 to 737 ng/dL and free testosterone by 38%, more than placebo with the same training but not more than placebo with double training. In the 40-man trial free testosterone rose 17% while placebo fell slightly. No libido or other symptom outcome was measured.

Endurance and time to exhaustion

In the 40-man trial, treadmill time to exhaustion rose 24.9% vs 10.3% on placebo, but the groups started unevenly (19.4 vs 22.4 minutes) and finished at about the same time (24.2 vs 24.8 minutes). In the 99-man trial, repetitions to failure on leg extension improved at both doses vs single-set placebo, but not vs the double-training placebo group.

Mechanism of action

1

Proposed mechanism: mTOR signalling (cell and rat data only)

Neither human trial measured muscle protein synthesis, mTOR, nitric oxide or oxidative stress. A cell and rat study of the same blend from the maker's laboratory reported PI3K/AKT/mTOR activation, more endothelial nitrite and less muscle loss in rats given dexamethasone. Cortisol fell 21% in the 40-man trial but did not change from baseline in any group in the 99-man trial. How the blend might affect testosterone has not been studied.

Clinical trials

1
RipFACTOR® (LI12542F6) for strength and endurance: 40-man trial
PubMed

Randomized, double-blind, placebo-controlled 56-day trial of LI12542F6 (650 mg/day) with a fixed resistance training program, registered CTRI/2016/05/006950 and funded by Laila Nutraceuticals. Outcomes: 1RM bench and leg press, handgrip, cable pull-down reps, treadmill time to exhaustion, DEXA body composition, free testosterone, DHT and cortisol. (Rokkam et al. 2023, Food Nutr Res)

40 recreationally active men aged 18 to 40 (20 per group), single site in Vijayawada, India.

At day 56: bench press 1RM +27.6 kg vs +5.0 kg on placebo, leg press +29.5 kg vs +5.7 kg, handgrip +13.6 kg vs +10.6 kg, cable pull-down reps +5.1 vs +2.6, treadmill time +4.8 vs +2.3 minutes (groups unequal at baseline), lean mass +1.44 kg vs +0.02 kg, fat mass -0.97 vs -0.20 kg, free testosterone +17% vs a slight fall, cortisol -21%. DHT did not differ between groups. No adverse events; safety labs stayed in normal ranges. Limits: small, single site, sponsor-funded, diet not controlled, total testosterone not measured.

2
RipFACTOR® at two doses vs single and double training: 99-man trial
PubMed

56-day, four-arm, randomized, blinded, placebo-controlled trial of a water-dispersible version of the blend at 425 or 850 mg/day with one training set, against placebo with one set or two sets; registered CTRI/2018/12/016641, funded by General Nutrition Centre Inc., first author employed by PLT Health Solutions. (Salter et al. 2024, Front Nutr)

120 previously untrained men aged 19 to 29 randomized, 99 completed (analysed n = 26, 25, 25, 23), single site in Bengaluru, India.

Versus single-set placebo at day 56, the 425 and 850 mg arms bench pressed 10.6 and 13.8 kg more, with leg extension and total strength also higher. Versus double-set placebo, both doses led on leg extension and total strength, but only 850 mg led on bench press (9.9 kg, p = 0.010; 425 mg: 6.8 kg, p = 0.166). Total and free testosterone beat single-set placebo but not double-set placebo. The two placebo groups never differed significantly. Eight minor adverse events, evenly split, none serious.

Side effects and drug interactions

Common Potential side effects

Well tolerated in both 56-day trials: no adverse events in the 40-man trial and eight minor ones, evenly split between supplement and placebo, in the 99-man trial. Blood counts, liver and kidney tests and lipids stayed within normal ranges.
No trial has enrolled women, so effects and safety in women, including in pregnancy or breastfeeding, are unknown; avoid use in pregnancy or while nursing.
Studied only in men aged 18 to 40; there are no data in teens or older adults.
In rat safety studies of the same extract there was no genetic toxicity and no adverse effect at up to 2,000 mg/kg/day for 90 days; a 28-day study showed stomach-lining irritation at 1,000 and 1,500 mg/kg/day that eased during recovery. Human data cover 56 days only.

Important Drug interactions

Testosterone therapy or anabolic drugs: possible additive effect on androgen levels; not studied, and both trials excluded men using them.
5-alpha reductase inhibitors (finasteride, dutasteride): interaction not studied. Sphaeranthus indicus extracts inhibited 5-alpha reductase in lab tests and reduced testosterone-induced prostate growth in rats, while DHT did not change versus placebo in the 40-man trial.
No drug-interaction or pharmacokinetic studies of this blend have been published.

Frequently asked questions about RipFACTOR® (Sphaeranthus + Mango Bark Blend for Muscle Strength — PLT Health)

What is RipFACTOR?

RipFACTOR® is a branded blend of Sphaeranthus indicus (East Indian globe thistle) flower head extract and Mangifera indica (mango tree) bark extract, developed by Laila Nutraceuticals and sold by PLT Health Solutions.

What is RipFACTOR used for?

RipFACTOR is researched primarily for Athletic Performance, Muscle & Recovery, and Testosterone. In 40 recreationally active men taking 650 mg/day for 8 weeks, bench press 1RM rose 27.6 kg vs 5.0 kg on placebo and leg press 29.5 kg vs 5.7 kg, unusually large gains for any supplement. In 99 previously untrained men, 850 mg/day added 13.

What is the recommended dosage of RipFACTOR?

The clinically studied dose is Tested: 650 mg/day of LI12542F6 for 56 days, or 425 or 850 mg/day of a water-dispersible version; the two were standardized differently, so equal mass is not an equal marker dose. Always follow the product label and check with a healthcare provider for personal advice.

Is RipFACTOR safe, and does it have side effects?

Side effects and cautions reported for RipFACTOR include: Well tolerated in both 56-day trials: no adverse events in the 40-man trial and eight minor ones, evenly split between supplement and placebo, in the 99-man trial. Blood counts, liver and kidney tests and lipids stayed within normal ranges. It may also interact with some medications. RipFACTOR is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does RipFACTOR interact with any medications?

Possible interactions include: Testosterone therapy or anabolic drugs: possible additive effect on androgen levels; not studied, and both trials excluded men using them. 5-alpha reductase inhibitors (finasteride, dutasteride): interaction not studied. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for RipFACTOR?

NutraSmarts rates the evidence for RipFACTOR as Limited (2 out of 5). It is backed by 2 study summaries and 6 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(6 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Salter D, Swamy S, Salis KM, Deep DK, Nadig P. A botanical extract blend of Mangifera indica and Sphaeranthus indicus combined with resistance exercise training improves muscle strength and endurance over exercise alone in young men: a randomized, blinded, placebo-controlled trial. Front Nutr. 2024;11:1393917. doi: 10.3389/fnut.2024.1393917.PubMedUsed to support: Four-arm, 56-day randomized blinded trial in 99 previously untrained men (19 to 29) in Bengaluru, India. Both doses (425 and 850 mg/day) gained more bench press, leg extension and total strength than placebo with one training set; against placebo with two sets, both led on leg extension and total strength but only 850 mg led on bench press (9.9 kg, p = 0.010). Total and free testosterone beat single-set but not double-set placebo; the two placebo groups never differed significantly. Funded by General Nutrition Centre Inc.; first author employed by PLT Health Solutions.
  2. Rokkam MP, Gora O, Konda MR, Koushik A. A proprietary blend of Sphaeranthus indicus flower head and Mangifera indica bark extracts increases muscle strength and enhances endurance in young male volunteers: a randomized, double-blinded, placebo-controlled trial. Food Nutr Res. 2023;67:8972. doi: 10.29219/fnr.v67.8972.PubMedUsed to support: Laila Nutraceuticals-funded 56-day randomized trial in 40 recreationally active men (18 to 40) in Vijayawada, India, testing 650 mg/day LI12542F6. Bench press 1RM went from 42.9 to 49.4 kg by day 14 (placebo 44.45 to 44.60 kg); by day 56 gains were 27.6 vs 5.0 kg on bench press and 29.5 vs 5.7 kg on leg press, with more lean mass (+1.44 kg), free testosterone +17% and cortisol -21%. Treadmill time results depend on a baseline-adjusted analysis because the groups started unequal. Diet was not controlled; no adverse events.
  3. Nahata A, Dixit VK. Sphaeranthus indicus attenuates testosterone induced prostatic hypertrophy in albino rats. Phytother Res. 2011;25(12):1839-48. doi: 10.1002/ptr.3497.PubMedUsed to support: Rat study of Sphaeranthus indicus extracts (not the branded blend): the extracts reduced testosterone-induced prostate enlargement, with finasteride as the comparison. Animal data only, suggesting anti-androgen activity in the prostate.
  4. Nahata A, Dixit VK. Evaluation of 5alpha-reductase inhibitory activity of certain herbs useful as antiandrogens. Andrologia. 2014;46(6):592-601. doi: 10.1111/and.12115.PubMedUsed to support: Lab enzyme screen in which Sphaeranthus indicus extract was one of five herbs identified as promising 5-alpha reductase inhibitors. In vitro only, unstandardized extract, no human data.
  5. Nestmann ER, Alluri VK, Dodda S, Davis BA. Toxicological studies on the botanical supplement LI12542F6 containing extracts of Sphaeranthus indicus flower heads and Mangifera indica (mango tree) bark. Food Sci Nutr. 2019;7(2):817-833. doi: 10.1002/fsn3.931.PubMedUsed to support: GLP toxicology studies of LI12542F6: no bacterial mutagenicity or mouse bone marrow genotoxicity, oral LD50 above 2,000 mg/kg, and a 90-day rat NOAEL above 2,000 mg/kg/day. The 28-day rat study found forestomach irritation at 1,000 and 1,500 mg/kg/day that lessened in recovery and was absent at 90 days; the extract is an eye irritant. Two of four authors work for Laila Nutraceuticals and PLT Health Solutions.
  6. Kundimi S, Rao T, Park GD, Kim KS, Kim SR, Alluri KV, Sengupta K. A standardized combination of Sphaeranthus indicus and Mangifera indica extracts improves antioxidant defense and anabolic signaling and attenuates dexamethasone-induced skeletal muscle atrophy. Food Nutr Res. 2026;70:14578. doi: 10.29219/fnr.v70.14578.PubMedUsed to support: Cell and rat study of the LI12542F6 blend by the maker's scientists: PI3K/AKT/mTOR activation, more endothelial nitrite, and preserved lean mass and grip strength in dexamethasone-treated rats at 45 and 90 mg/kg. Not a human study; the authors call for clinical confirmation.