[Latin Name] Cinnamomun camphcra

[Plant Source] It is extracted from Ginkgo Biloba Leaf.

[Specifications]

1, Ginkgo Biloba Extract 24/6

Total Ginkgo flavone glycosides 24%

Total terpene lactones 6%

2, Ginkgo Biloba Extract 24/6

Total Ginkgo flavone glycosides 24%

Total terpene lactones 6%

Ginkgolic acid 5ppm

3,CP2005

Total Ginkgo flavone glycosides 24%

Quercatin: kaemperol 0.8–1.5

Total terpene lactones 6%

Ginkgolic acid <5ppm

4.Germany Standard

Total Ginkgo Flavone Glycosides 22.0%-27%

Total Terpene Lactones 5.0%-7.0%

Bilobalides 2.6%-3.2%

Ginkgolic acid <1ppm

5.Water-Soluble Ginkgo Biloba Extract 24/6

Water Solubility: 5g Ginkgo Biloba Extract will be dissolved completely in 100g water

Total Ginkgo Flavone Glycosides 24.0%

Total Terpene Lactones 6.0%

Ginkgolic acid <5.0ppm

[Appearance] Light yellow fine powder

[Particle size] 80 Mesh

[Loss on drying] £ 5.0%

[Heavy Metal] £10PPM

[Extract solvents] Ethanol

[Storage] Store in cool & dry area, keep away from the direct light and heat.

[Package] Packed in paper-drums and two plastic-bags inside.

[Function]

Expanding blood vessel, resisting insufficient blood and oxygen deficit, increasing blood flow, improving cerebral arteries and distal

blood flow. Promoting cerebral circulation metabolism, improving memory function, resisting depression, resisting lipidic overoxidation,

protecting liver damage.

In clinic, curing high blood pressure, hyperlipoidemia, coronary heart disease, angina pectoris, arterial sclerosis, cerebral embolism,

senile dementia, primary and periodic dropsy, acute drumming in the ears, epicophosis, a variety of body function in disorder, dizziness

and so on.

Heres the list people….
Methadone-oral 80-90%, halflife- 24-36 hours, rectal 76%
Ketobemiodone oral was 34% +/-10%, rectally 44% +/- 9%, half-life is 2.25- 2.45 hours
Meperidine rectal bioavailability is approximately 55%, 80% to 85% IM, elimination half-life 3.0 h
Buprenorphine highly protein bound 96%, sublingual bioavailability is approximately 30%, oral is 15-22%, 90-100% IM, elimination half-life is 12-44 hours
Hydromorphone– 5-8 times as potent as morphine, intranasal- 52.4%, Rectal administration 33% ,Oral-30-35%, (also reported as 50.7% +/- 29.8% oral; 33% +/- 22% rectal; 54.4% – 59.8% nasal)
Dihydrocodeine oral-20-21% halflife 4 hours
Heroin oral ~35% IV- 100% IM-85% Smoked (or vaporized?) 52-55% vaporized Semisynthetic derivative, Intranasal 44-61%
Fentanyl- Bioavailability 92% (transdermal), 50% (sublingual/ buccal (against cheek), Protein binding 80-85%, half-life 3-12 hours
Sufentanil intranasal bio- 78%,
Remifentanil Protein binding 70% (bound to plasma proteins) Half life 1-20 minutes
Alfentanil- IV ~100%, 92% protein binding, half life is 1.5-2 hours
Morphine ~32% oral/rectal, insuffulated- 15-20%, Chitosan(a linear polysaccharide that helps absorb drugs better) has been shown to increase nasal bioavailability of morphine from around 10-20% to over 60%, SC-60%, protein binding 30-40%, half-life is 2-3 hours
Oxycodone-oral 60-87% intranasal- widely varies 45-70%
Hydrocodone- oral bioavailability is not really known but it is around oxycodone bioavailability, ~70% of it is usually absorbed, half-life is 4-8 hours
Oxymorphone nasal bioavailabilty [43%] orals low 10-20%
Butorphanol -oral 5-17% due to high first pass metabolism
Tramadol- the absolute bioavailability of rectally admistered tramadol in the suppositories was 77.0%, Oral-68-72% (Increases with repeated dosing) Half life 5-7 hours
Codeine- following rectal or oral administration with a systemic availability of about 90%; in one study clearance varied 4-fold and systemic availability after oral dosage was between 50 and 84%
Diphenoxylate Protein binding 74-95% Half life 12-14 hours used for diarrhea, (does not appreciably cross the blood-brain barrier)
Pethidine(meperidine) Absorption Oral bioavailability is 50-60% in patients with normal hepatic function. IM 80-85%, Protein Binding 65-75%, Half Life 3-5 hours
Normeperidine is about half as potent as meperidine, but it has twice the CNS stimulation effects.
Pentazocine- Bioavailability ~20% orally, Half-life 2 to 3 hours

Opiate Antagonists
Naloxone oral- 2-4% (90% absorption but high first-pass metabolism), Half life 1-1.5 hours
Naltrexone Oral Bioavailability 5-40%, Protein binding 21%, Half life-4 hours (naltrexone),
and 13 hours (6-β-naltrexol) (metabolite)

●▬▬๑۩۩๑▬▬●READ ME!!!! ●▬▬๑۩۩๑▬▬●

Never do this to your face. I tried it once in 2011 and I am lucky I didn’t develop permanent scarring. I read a lot of threads on different forums about this peel and turned into a kitchen beautician. No no no.

Not sure why my tca video gets lumped in with the bleaching videos, but due to the foolishness, I had to disable comments. ANywho, in the description box tells the details…a lot more than I talk about in the video. I tried this once,and decided it wasn’t for me and haven’t done another since. In fact I actually stick to exfoliating cleansers and rose hip oil now

Pics at 2:20!

I tried this tca peel out in 2011. These pictures are about 2 years old from when this video was made.

Chemical peels can be done on the face, neck, or hands. They can be used to:

•Reduce fine lines under the eyes and around the mouth
•Treat wrinkles caused by sun damage and aging
•Improve the appearance of mild scars
•Treat certain types of acne
•Reduce age spots, freckles, and dark patches (melasma)
•Improve the look and feel of skin

So in this vlog, I talk about my tca peeling. Girl, I told ya’ll it was bad. HA! But to be honest, this is actually normal for dark skin like mine. It get worse before it gets better! Some people would rather cover up their scars and blemishes with makeup, but I wanted to do something about the skin itself, since makeup only masks the problem.

I ordered my 12% solution tca peel from https://www.makeupartistschoice.com/. I also first did a skin test on a small patch to make sure I wasn’t allergic or had any adverse reaction to the acid.

Yes, it hurt/burned. It’s a stronger acid than gycolic or lactic so you will definately feel it. I kept a fan in front of my face while I applied to take away some of the sting, but I still felt it. I recommend a few ibuprofen 15 min before to buffer the discomfort.

It took about a full month for my skin to completely recover. About 3-4 days for the top layer of skin that was treated with the chemical to darken and begin to peel, another 3-6 days of peeling.

This was a slow process because you want it to happen organically and not pull the dried, flaky skin off because that can cause hyperpigmentaion and scarring.

After the skin was all off, it took a good 2 weeks for the pink new fresh skin to darken back to my natural color. I used polysporin and sunscreen everyday and kept my face clean and moist with ointment for optimal healing.

I’m doing good on my juicing and raw eating. My thighs are on fire from my workouts and all is well.

Happy Sunday!

Hurr: Janet Collection Whole Lace Dior Wig
Eyes: EOS Ice Brown circle lenses
Lipz: Maybelline ColorSensational Vivids Lipcolor, Pink Pop
Music: Sweet Nothing-Clavin Harris(ft. Florence Welch) instrumental