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Facebook: https://www.facebook.com/expertclipping
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Free quote: https://www.expertclipping.com/free-quote/
Pricing & Payments: https://www.expertclipping.com/pricing/
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Office address:
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Phone: +880 1711011258
UK OFFICE
24 Longbridge Road
Barking Essex IG118tnv
www.expertclipping.co.uk
Phone: 02036093822
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168 Belaws, 4th Floor
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A Ret 0.05% Gel (Tretinoin 0.05%)
About A RET 0.05% GEL
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A RET 0.05% GEL 15GM is available in both topical and oral dosage form. The oral form of A RET 0.05% GEL 15GM should be taken as prescribed by your doctor. A topical form of A RET 0.05% GEL 15GM can be taken on the fingertip and applied on the clean and dry affected area. Avoid contact of A RET 0.05% GEL 15GM with nose, mouth, eyes, ears or vagina. In case A RET 0.05% GEL 15GM comes in contact with these areas accidentally, rinse with water thoroughly. Some people may experience dry skin, peeling, redness, burning, itching or stinging sensation of the skin. Most of these side effects of A RET 0.05% GEL 15GM do not require medical attention and gradually resolve over time. However, if the side effects persist or worsen, please consult your doctor.
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Other dosage
A ret 0.025%
A ret 0.5%
A ret 0.1%
A Ret HC Cream
Uses
Acne, Wrinkles, Leukemia (blood cancer)
Medicinal Benefits
ARET 0.05% GEL 15GM is a form of vitamin A (retinoid) that loosen and unblock pores in the skin’s surface by reducing the oil secretion in the skin. This prevents the formation of pimples, whiteheads and blackheads. ARET 0.05% GEL 15GM also reduces the excessive production of abnormal blood cells and stimulates the growth of normal, mature cells in blood and bone marrow. So, in the oral form, ARET 0.05% GEL 15GM is used in the treatment of leukaemia (a type of blood cancer).
Directions for Use
Topically: Wash your hands before and after applying ARET 0.05% GEL 15GM. Before using it, try to clean and dry the affected skin area. Applying ARET 0.05% GEL 15GM to wet skin may cause skin irritation, so try not to wash the treated area. Also do not apply other skin products for at least 1 hour after applying ARET 0.05% GEL 15GM. Wash the face with mild soap and pat the skin dry. Take a small pearl-sized amount of ARET 0.05% GEL 15GM on the fingertip and apply on the clean and dry affected area once a day in the evening. Avoid contact of ARET 0.05% GEL 15GM with nose, mouth, eyes, ears or vagina. In case ARET 0.05% GEL 15GM comes in contact with these areas accidentally, rinse with water thoroughly. Orally: If you are prescribed ARET 0.05% GEL 15GM in oral form, swallow the whole capsule with a glass of water. Take ARET 0.05% GEL 15GM with food to avoid stomach upset. Do not break, crush or chew it.
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Buy ADB-FUBINACA Powder
Buy ADB-FUBINACA Powder is a designer drug identified in synthetic cannabis blends in Japan in 2013. In 2018, it was the third-most common synthetic cannabinoid identified in drugs seized by the Drug Enforcement Agency.
The (S)-enantiomer of ADB-FUBINACA is described in a 2009 Pfizer patent and has been reported to be a potent agonist of the CB1 receptor and the CB2 receptor with EC50 values of 1.2 nM and 3.5 nM, respectively. ADB-FUBINACA features a carboxamide group at the 3-indazole position, like SDB-001 and STS-135. ADB-FUBINACA appears to be the product of rational drug design, since it differs from AB-FUBINACA only by the replacement of the isopropyl group with a tert-butyl group.
An analogue of ADB-FUBINACA, ADSB-FUB-187, containing a more functionalized carboxamide substituent was recently reported.
Technical Information
Formal Name: N-[1-(aminocarbonyl)-2,2-dimethylpropyl]-1-[(4-fluorophenyl)methyl]-1H-indazole-3-carboxamide
CAS Number: 1445583-51-6
Molecular Formula: C21H23FN4O2
Formula Weight: 382.4
Purity: ?98%
Formulation: A neat solid
SMILES: O=C(NC(C(N)=O)C(C)(C)C)C1=NN(CC2=CC=C(F)C=C2)C3=C1C=CC=C3
InChi CodeInChI=1S/C21H23FN4O2/c1–21(2,3)18(19(23)27)24-20(28)17-15-6-4-5-7-16(15)26(25-17)12-13-8-10-14(22)11-9-13/h4-11,18H,12H2,1-3H3,(H2,23,27)(H,24,28)
InChi Key: ZSSGCSINPVBLQD-UHFFFAOYSA-N
DEA Schedule: I
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Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 3 years
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In the United States, ADB-FUBINACA is a Schedule I controlled substance.
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Twenty-three ADB-FUBINACA major metabolites were identified in several incubations with cryopreserved human hepatocytes. Major metabolic pathways were alkyl and indazole hydroxylation, terminal amide hydrolysis, subsequent glucuronide conjugations, and dehydrogenation
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One death through coronary arterial thrombosis has been linked to ADB-FUBINACA intoxication.
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