Jacek Olczak - Philip Morris International, Inc.
Management
Chris, we have said – it's Jacek here, we have said that we look to grow the revenues above the 6% or the upper-end of the current (42:45) and clearly still we're lifting EPS. So, you could see that we are not diluting the margins. I think we should look for the year when we will have a small but still the margin expansion operating profit margin expansion, not to the tune which we had in 2016. André mentioned that there is a device sales in this revenue and, for a time being, they yield a negative margin. So, that's obviously dilutive. But the HeatSticks, and still the performance of the combustibles were both (43:18) 6% pricing. I mean, that should allow us for some margin expansion, say 10, 20 basis points, and we will see how the year unfolds.
Christopher Growe - Stifel, Nicolaus & Co., Inc.: Okay. And then just one other follow-up question, if I could, which is that, if you were able to get approval as a Modified Risk Tobacco Product in the U.S. in 2017, I'm just curious what that would mean to you in other international markets, in Japan? I'm obviously getting to – could you make a, or would you make, a claim and would that, for some reason, cause you to accelerate your investments in IQOS?
André Calantzopoulos - Philip Morris International, Inc.: Okay, Chris. First of all, it is highly unlikely we will get approval for MRTP in 2017.
Christopher Growe - Stifel, Nicolaus & Co., Inc.: Yes.
André Calantzopoulos - Philip Morris International, Inc.: Okay. As you know, the FDA gave a guidance that they would – may take X-days, but I mean that may take more time. What we believe is more within the 2017 realm, is the product authorization for the U.S. market without claims, okay. And we will submit that application, the PMTA application, in the first quarter this year, okay. Now, irrespective of the approval in the U.S. – the FDA approval obviously helps the credibility internationally, but it doesn't apply to Japan, okay.
Christopher Growe - Stifel, Nicolaus & Co., Inc.: Yeah.
André Calantzopoulos - Philip Morris International, Inc.: In Japan and other markets, our claim structure, as we said, follows the local legislation, but also the conclusion of our own science. So, what we communicate to the consumers is driven by local laws and our own science. And the FDA cannot be applied to these places. But, obviously, it will add credibility to their entire scientific dossier, and that's why it is important to us.
Christopher Growe - Stifel, Nicolaus & Co., Inc.: Okay. Thank you for your time.
André Calantzopoulos - Philip Morris International, Inc.: You're welcome.