C4 Laboratories, LLC 1930 S. Alma School Rd Suite B202 Mesa, AZ "Patient protection through true science" Dear Valued Colleague,

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Dear Valued Colleague, C4 Laboratories, LLC 1930 S. Alma School Rd Suite B202 Mesa, AZ 85210 www.c4lab.com "Patient protection through true science" Thank you for selecting C4 Laboratories. Our goal at C4 is to provide reliable data that is interpreted within the appropriate physiological context, to ultimately empower patients to use cannabis medicine more effectively. The data within this report are the result of various analytical methods that have been developed by the team of scientists at C4 Laboratories. For the characterization and quantification of 21 terpene compounds and residual solvents we use Head- Space Gas Chromatography with Flame Ionization Detection (HS- GC- FID). Additionally, Ultra High Performance Liquid Chromatography (UHPLC) is used for the characterization and quantification of the 10 major phytocannabinoids found in cannabis. All data are collected in concert with proper quality assurance/quality control measures (QA/QC), including the use of intermittent analytical blanks, sample spikes, and commercial standards. As an additional measure of quality control, we provide a historical reference (when available) to analytical results from an equivalent strain of cannabis/cannabis product to draw comparison. We understand that within an individual strain that results may vary as a result of variances in sample homogeniety, analytical methodology, crop conditions, genetic drift, and/or gene flow during hybridization. However, such a comparison can provide valuable insight into sample integrity and/or the phenotypic identity of the analyzed sample. Additionally, we have interpreted all data within the physiological context provided to us by the growing body of peer- reviewed scientific research studies. Key factors to consider when determing how to most appropriately use a particular strain of cannabis include, but are not limited to, an evaluation of the possible cannabinoid/terpene synergies and an analysis of the various cannabinoid ratios, particular the CBD- A/THC- A and CBG/CBN ratios. It is important to note that when analyzing cannabis there can exist natural variablity of cannabinoid and terpene concentrations within individual plants. Cannabinoid concentrations in cannabis flower have been found to increase distally with respect to the root mass. As such, the analysis of multiple samples from any plant of interest is recommended. Thank you again for your confidence in C4 Laboratories. We strive to be an authority on cannabis education, targeted therapies and patient protection. Also, as a research laboratory, we hope to discover novel cannabis constituents through our efforts with academic research programs in the C4 Cannabinomics Collaborative. For more information about how you can collaborate with our research team please visit our website at www.c4lab.com. Zacariah L. Hildenbrand, Ph.D. Chief Scientific Officer C4 Laboratories, LLC

PRODUCT SUMMARY ID: EC_XI8_121015 Analyte: Flower Strain: XI8 Client: Errl Cup Date: 12/10/15 Microbial Screen: PASS Foreign Material: PASS Pesticide Analysis: Not performed Residual Solvents: Not performed 18.08% Major 10 Cannabinoids: Total available THC: 15.50% Total THC Isomers: 15.50% Δ9 + Δ8 THC Total available CBD: 0.00% Highest Terpenes: Not performed Not performed Not performed Activated THC: 0.000 (mg) APPLICABLE TO MEDIBLES, TINCTURES AND SALVES Fresh product CBG/CBN > 1.0 denotes fresh product, CBG/CBN < 1.0 denotes high CBN 0.00 (CBG/CBN): strain and/or an oxidized product Targeted Use: Appetite stimulant (CBN), anti- inflammatory and analgesic (THC)

Potency Profile Value (%) Historical (%) CBDV Therapeutic properties CBD- A CBG CBD THCV CBN Δ9- THC Δ8- THC 0.58 #N/A 1.25 #N/A Appetite stimulant (Farrimond et al., 2012), analgesic (Zygmunt et al., 2002) and anti- tumorigenic against some forms of lung cancer (BiFulco et al., 2006) Anti- inflammatory and analgesic (Russo, 2011), neuroprotectant (Hampson et al., 1999), reduces intraocular pressure associated with glaucoma, spasticity and muscle tension (Pacher et al., 2006) CBC Δ9- THC- A 16.26 #N/A Total Available THC 15.50 #N/A Total THC Isomers 15.50 #N/A Total Available CBD CBD/Δ9- THC ratio CBG/CBN ratio Major 10 Total 18.08 #N/A See therapeutic properties of Δ9- THC for medicinal value upon activation through decarboxylation General Characteristics Δ9- THC- A + Δ9- THC (accounts for conversion rate) Δ9- THC- A + Δ9- THC + Δ8- THC (accounts for conversion rate) CBD- A + CBD (accounts for conversion rate) THC- dominant, psychoactive CBG/CBN > 1.0 denotes fresh product, CBG/CBN < 1.0 denotes high CBN strain and/or an oxidized product Historical measurements based on analysis of equivalent product N/A #N/A Blank cells denote cannabinoid concentrations below the limit of detection (0.01%) #N/A

Terpene Profile Value (%) Historical (%) Therapeutic properties alpha- Pinene Camphene beta- Pinene beta- Myrcene delta- 3- Carene alpha- Terpinene p- Cymene d- Limonene Ocimene gamma- Terpinene Terpinolene Linalool (- )- Isopulegol Geraniol beta- Caryophyllene alpha- Humulene Nerolidol Guaiol (- )- alpha- Bisabolol Eucalyptol (- )- Caryophyllene oxide Terpene Total #N/A * Based on historical measurements of equivalent strain/product Blank cells denote terpene concentrations below the limit of detection (0.001%)

Cannabinoid Ratios CBD- A/Δ9- THC- A ratio is outide of the optimal therapeutic range of 1-2 (Lemberger et al., 1976; Burnett, 2014) CBD- A/Δ9- THC- A ratio is below 1, user may experience tachycardia (increased heart rate) and difficulty walking, resulting from elevated THC (Burnett, 2014) CBG/CBN > 1.0 denotes fresh product and is useful for the treatment of gastrointestinal abnormalities (Borrelli et al., 2013), CBG/CBN < 1.0 denotes high CBN strain and/or an oxidized product Cannabinoid/Terpene Synergies (Russo, 2011) Additional Observations Terpene analysis was not performed Residual Solvents Not performed Pesticides Not performed

References G. Appendinoa et al., "NPC Natural Product Communications 2008," NPC Natural Product Communications: 1977. M. Backes, "Cannabis Pharmacy," 2014. F. Bettarini et al., "Antiparasitic compounds from East African plants: isolation and biological activity of anonaine, matricarianol, canthin- 6- one, and caryophyllene oxide," Insect Sciences and Applications 14, 1993. M. BiFulco et al., "Cannabinoids and cancer: pros and cons of an antitumor strategy," British Journal of Pharmacology 148, 2006. L. Binet et al., "Recherches sur les proprietes pharmacodynamiques de quelques alcools terpeniques aliphatiques," Ann Pharm Fr 30, 1972. F. Borrelli et al., "Beneficial effect of the non- psychotropic plant cannabinoid cannabigerol on experimental inflammatory bowel disease, " Biochemical Pharmacology 85, 2013. G. Buchbauer et al., "Fragrance compounds and essential oils with sedative effects upon inhalation," Journal of Pharmacological Sciences 82, 1993. M. Burnett, "Finding the optimal therapeutic ratio of THC and CBD," www.medicaljane.com, 2014. W.E. Campbell et al., "Composition and anti- malarial activity in vitro of essential oil of Tetradenia riparia," Planta Med 63, 1997 G.T. DeLong et al., "Pharmacological evaluation of the natural constituent of Cannabis sativa, cannabichromene and its modulation by delta- 9- tetrahydrocannabinol," Drug Alcohol Dependence 112, 2010. R. Deyo and R. Musty, "A cannabichromene (CBC) extract alters behavioral despair on the mouse tail suspension test of depression," Proceedings 2003 Symposium on the Cannabinoids (Cornwall, ON: International Cannabinoid Research Society, 2003) A.T. El- Alfy et al., "Antidepressant- like effect of delta- 9- tetrahydrocannabinol and other cannabinoids isolated from Cannabis sativa," Pharmacological Biochemical Behavior 95, 2010. E. Elisabetsky et al., "Effects of linalool on glutamatergic system in the rat cerebral cortex," Neurochemical Research 20, 1995. H.N. ElSohly et al., "Synthesis and antimicrobial activities of certain cannabichromene and cannabigerol- related compounds," Journal of Pharmaceutical Sciences 71, 1982. A.A. Falk et al., "Uptake, distribution and elimination of alpha- pinene in man after exposure by inhalation," Scandinavian Journal of Work and Environmental Health 16, 1990. J.A. Farrimond et al., "Cannabinol and cannabidiol exert opposing effects on rat feeding patterns," Psychopharmacology 223, 2012. M.L. Gil et al., "Comparative study of different essential oils of Bupleurum gibraltaricum lamarck," Pharmazie 44, 1989. A.J. Hampson et al., "Cannabidiol and delta- 9- tetrahydrocannabinol are neuroprotective antioxidants." Proceedings of the National Academy of Sciences of the United States 14, 1998. B. Harris, "Phytotherapeutic uses of essential oils," Handbook of Essential Oils: Science, Technology and Application. CRC Press, pp:315-352, 2010. A.A. Izzo et al., "Inhibitory effect of cannabichromene, a major non- psychotropic cannabinoid extracted from Cannabis sativa, on inflammation- induced hypermotility in mice," British Journal of Pharmacology 166, 2012. N.A. Jones et al., "Cannabidiol displays antiepileptiform and antiseizure properties in vitro and in vivo," Journal of Pharmacology and Experimental Therapeutics 332, 2010. S.S. Kim et al., "Biological activities of Korean citrus obovoides and citrus natsudaidal essential oils against acne- inducing bacteria," Bioscience Biotechnology and Biochemistry 72, 2008. T. Komori et al., "Effects of citrus fragrance on immune function and depressive states," Neuroimmunomodulation 2, 1995, L. Lemberger et al., "Clincial studies on the interaction of psychopharmacologic agents with marijuana," Ann NY Academia Sciences 281, 1976. N.P. Lopes et al., "Antimalarial use of volatile oil from leaves of Virola surinamensis," Journal of Ethnopharmacology 67, 1999. P. 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Russo, "Taming THC: Potential cannabis synergy and phytocannabinoid- terpenoid entourage effects," British Journal of Pharmacology 163, 2011. E.B. Russo and G.W. Guy, "A tale of two cannabinoids: the therapeutic rationale for combining tetrahydrocannabinol and cannabidiol," Medical Hypotheses 66, 2006.

S. Sarfaraz et al., "Cannabinoids for cancer treatment: progress and promise," Cancer Research 68, 2008. N. Shingyo and V. Di Marzo, "The effect of cannabichromene on adult neural stem/progenitor cells," Neurochemistry International 63, 2013. Y. Tambe et al., "Gastric cytoprotection of the non- steroidal anti- inflammatory sesquiterpene, beta- caryophyllene," Planta Med 62, 1996. T.G. do Vale et al., "Central effects of citral, myrcene and limonene, constituents of essential oil chemotypes from Lippia alba," Phytomedicine 9, 2002. D.M. Vigushin et al., "Phase I and pharmacokinetic study of d- limonene in patients with advanced cancer," Cancer Chemotherapy Pharmacology 42, 1998. E.T. Wargent et al., "The cannabinoid delta- 9- tetrahydrocannabivarin (THCV) ameliorates insulin sensitivity in two mouse models of obesity," Nutritional Diabetes 27, 2013. D. Yang et al., "Use of caryophyllene oxide and an anti- fungal agent in an in vitro experimental model of onychomycosis," Mycopathologia 148, 1999. P.M. Zygmunt et al., "delta- 9- tetrahydrocannabinol and cannabinol activate capsaicin- sensitive sensory nerves via a CB1 and CB2 cannabinoid receptor- independent mechanism," Journal of Neuroscience 22, 2002. V. Corpas- Lopez et al., "a- Bisabolol, a promising oral comppund for the treatment of visceral leishmaniasis." J Natural Products 78, 2015. S. Kim et al., "Dietary camphene attentuates hepatic steatosis and insulin resistance in mice," Obesity 2, 2014. M.A. Ocete, " Pharmacological activity of the essential oil of Bupleurum gibraltericum: anti- inflammatory activity and effects on isolated rat uteri," J. Ethnopharmacology 3, 1989. L. Chen et al., "Protective effect of p- cymene on lipopolysaccharide- induced acute lung injury in mice," Inflammation 37(2), 2014 A. Khan, "Eucalyptol mitigates inflammation in amyloaid Beta toxicated PC12 cells: relevance to Alzheimer's disease," Neurochemical Research 39(2), 2014. K. Medicherla, "Oral administration of geraniol ameliorates acute experiemental murine colitis by inhibiting pro- inflammatory cytokines and NF- kb signaling," Food Funct, 2015. M.A. Apel, "Anti- inflammatory activity of essential oil from leaves of Myrciaria tenella and Calycorectes sellowianus," Pharm Biol 48(4), 2010. A.P. Rogerio et al., "Preventative and therapeutic anti- inflammatory properties of the sesquiterpene alpha- humulene in experimental airways allergic inflammation," British J. Pharmacology 158(4), 2009. M.I. Silva, " Central nervous system activity of acute administration of isopulegol in mice," Pharmacol. Biochem. Behav. 88(2), 2007. C. Cavaleiro, "Antifungal activity of the essential oil of Angelica major against Candida, Cryptococcus, Aspergillus dermatophyte species," J Natural Medicine 69(2), 2015. T.R. Ramalho, "Gamma- Terpinene modulate acute inflammatory response in mice," Planta Medicine, 2015. H. Turkez, "Genotoxic and oxidative damage potentials in human lymphocytes after exposure to terpinolene in vitro," Cytotechnology 67(3), 2015. Questions regarding the results and/or the interpretations described within this report can be addressed to Zacariah Hildenbrand at zac@c4laboratories.com or 915-694- 7132

12/11/2015 10:48:36 AM Page 1 / 1 C4 Laboratories, LLC 1930 S. Alma School Rd Suite B202 Mesa, AZ 85210 www.c4lab.com "Patient protection through true science" C4 Laboratories, LLC Sample Name : XI-8 Sample ID : MeOH blank Data Filename : XI-8_007.lcd Method Filename : 10 Cannabinoids Standard Method mgperlv4.lcm Batch Filename : Batch v1.lcb Vial # : 1-34 Sample Type : Flower Injection Volume : 5 ul Date Acquired : 12/11/2015 10:31:44 AM Acquired by : Aaron J. Hicks Date Processed : 12/11/2015 10:38:45 AM Processed by : Sean S. Jun Cannabinoids by HPLC mau 250 200 150 THC-A / 16.257 % PDA Multi 1 220nm,4nm 100 50 CBN / 0.580 % THC / 1.247 % 0 1.0 1.5 2.0 2.5 3.0 3.5 4.0 4.5 5.0 min Cannabinoids PDA Ret. Time 2.739 3.210 3.606 Area 20114 26020 389275 Conc. CBD-V CBD-A CBG CBD THC-V 0.580% CBN 1.247% THC d8-thc CBC 16.257% THC-A Name C: LabSolutions Data 11 Dec 2015 XI-8_007.lcd